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Appendix A 225

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Appendix A

225

226

Ex

amin

atio

no

fd

rug

pri

ces

the

do

mes

tic

firm

sag

reed

tore

du

ce

Tabl

eA

.1V

olu

nta

ryp

rice

red

uct

ion

–m

arke

tp

rice

sve

rsu

scl

aim

edp

rice

s

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

305

187

13B

acip

en25

0A

nti

bact

eria

lC

ap10

30.8

028

.50

7.47

%3.

082.

852.

882.

88H

305

187

14B

acip

en50

0A

nti

bact

eria

lC

ap10

57.6

053

.00

7.99

%5.

765.

305.

385.

38H

191

15O

din

ol25

mg

Car

dio

vasc

ula

rTa

b14

11.5

08.

5026

.09%

0.82

0.61

0.71

H

191

16O

din

ol50

mg

Car

dio

vasc

ula

rTa

b14

19.0

016

.00

15.7

9%1.

361.

141.

25H

204

17A

lcep

hin

250

An

tiba

cter

ial

Cap

1062

.00

51.0

017

.74%

6.20

5.10

6.20

H

204

18A

lcep

hin

500

An

tiba

cter

ial

Cap

1011

0.00

95.5

013

.18%

11.0

09.

5511

.00

H

204

19A

lcep

hin

An

tiba

cter

ial

Dry

syru

p30

ml

23.8

521

.00

11.9

5%0.

80/m

l0.

70/m

l0.

70/m

lE

204

20A

lcep

hin

Kid

An

tiba

cter

ial

Tab

1029

.95

21.0

029

.88%

3.00

2.10

3.00

H

295

696

312

50A

lsig

ra50

An

tifu

nga

lsTa

b4

72.0

051

.00

29.1

7%7.

205.

107.

207.

207.

20H

268

273

72Fo

rmin

al10

00A

nti

dia

beti

csTa

b10

16.0

512

.50

22.1

2%1.

611.

251.

501.

50H

270

966

297

75Pi

olem

15A

nti

dia

beti

csd

rug

Tab

1018

.00

16.0

011

.11%

1.80

1.60

1.80

1.80

1.80

H

227

270

966

297

76Pi

olem

30A

nti

dia

beti

csd

rug

Tab

1035

.00

32.0

08.

57%

3.50

3.20

3.50

3.50

3.50

H

1,05

110

1Fo

lin

alp

lus

Iron

&V

itam

ins

sup

ple

men

tsSy

rup

300

ml

72.0

063

.50

11.8

1%0.

24/m

l0.

21/m

l0.

37/m

lH

312

180

111

Am

oxil

Am

oxyc

illi

nD

rysy

rup

30m

l25

.68

22.4

712

.50%

1.00

/m

l0.

86/m

l0.

47/m

l0.

49/m

lL

312

180

114

Am

oxil

250

mg

Am

oxil

cill

in25

0m

gC

ap20

×10

802.

5074

8.32

6.75

%4.

013.

743.

103.

58L

312

180

115

Am

oxil

500

mg

Am

oxil

cill

inC

ap20

×10

1510

.84

1337

.41

11.4

8%7.

556.

695.

905.

50L

528

164

Cad

flo

20m

gFl

uox

etin

eC

ap30

×10

C89

8.80

791.

8011

.90%

3.00

2.64

2.35

L

418

173

Cad

ith

ro50

mg

Rox

yth

rom

ycin

Tab

20×

10T

1005

.80

963.

004.

26%

5.03

4.82

4.70

L

418

174

Cad

ith

ro15

0m

gR

oxyt

hro

myc

inTa

b20

×10

T16

47.8

014

98.0

09.

09%

8.24

7.49

11.1

3H

476

825

212

176

Cet

icad

10m

gC

etri

zin

eH

Cl

Tab

50×

10T

1281

.86

805.

7137

.15%

2.56

1.61

2.60

2.60

2.60

H

188

548

236

178

Dom

coli

c10

mg

×D

omp

erid

one

Tab

50×

10T

1352

.48

1070

.00

20.8

9%2.

702.

142.

532.

532.

53H

373

479

184

Flu

med

150

mg

Flu

con

azol

eTa

b20

×1

684.

8057

7.80

15.6

3%34

.20

28.8

530

.00

26.0

0M

7362

926

419

0La

nzo

fast

30m

gLa

nso

pra

zole

asen

teri

c-co

ated

gran

ule

s

Cap

20×

10C

1070

.00

856.

0020

.00%

5.35

4.14

4.93

4.90

4.93

H

250

198

Nim

du

s-P

Nim

esu

lid

e10

0m

g+

Para

ceta

mol

500

mg

Tab

20×

10T

620.

6051

3.60

17.2

4%3.

102.

572.

90H

228

Tabl

eA

.1(C

onti

nu

ed)

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

250

199

Nim

du

s-Pl

us

Nim

esu

lid

e10

0m

g+

Para

ceta

mol

500

mg

Tab

50×

1015

51.5

010

86.0

530

.00%

3.10

2.17

2.90

H

354

201

Ori

ph

ex12

5D

TC

eph

alex

inTa

b20

×10

T62

8.95

588.

506.

43%

3.14

2.94

3.25

H

318

204

203

Ori

ph

ex25

0m

gC

eph

alex

inC

ap20

×10

C13

05.4

011

77.0

09.

84%

6.53

5.89

6.50

6.50

H

318

204

204

Ori

ph

ex50

0m

gC

eph

alex

inC

ap10

×10

C11

50.2

510

16.5

011

.63%

11.5

010

.17

12.1

012

.10

H

308

306

187

210

Zyci

llin

250

mg

Am

pic

illi

nTr

ihyd

rate

Cap

20×

10C

642.

0053

5.00

16.6

7%3.

212.

683.

003.

003.

00H

308

306

187

211

Zyci

llin

500

mg

Am

pic

illi

nTr

ihyd

rate

Cap

20×

10C

1241

.20

1070

.00

13.7

9%6.

215.

355.

805.

805.

80H

380

510

173

330

Zelb

end

400

mg,

Alb

end

azol

eI.

P.ex

cip

ien

tq

sTa

b20

×10

2675

.00

2247

.00

16.0

0%13

.38

11.2

310

.00

10.0

010

.00

L

409

404

Cad

imyc

etin

500

mg

Ch

lora

mp

hen

icol

Cap

10×

10C

730.

2864

2.00

12.0

9%7.

306.

426.

83H

409

405

Cad

imyc

etin

250

mg

Ch

lora

mp

hen

icol

Cap

20×

10C

770.

4066

3.40

13.8

9%3.

853.

313.

60H

229

1094

419

Cad

pro

250

gmG

BPr

otei

nG

ran

ule

s25

0gm

149.

7513

6.96

8.54

%0.

60/gm

0.55

/gm

0.50

/gm

L

155

148

239

425

Can

vas

5m

gEn

alap

ril

Tab

30×

1063

5.58

535.

0015

.82%

2.12

1.78

0.07

0.07

0.07

L31

849

5Zo

xLB

250

Am

oxyc

illi

n25

0m

g+

Lact

oB

acil

lus

Cap

10×

10C

406.

6032

1.00

21.0

5%4.

073.

213.

80H

318

496

Zox

LB50

0A

mox

ycil

lin

500

mg

+La

cto

Bac

illu

s

Cap

10×

10C

757.

5669

5.50

8.19

%7.

586.

967.

08H

380

508

173

501

Alz

adSu

spen

sion

Alb

end

azol

e5

ml-

IP-

200

mg

Liq

uid

10m

lB

ot21

.61

17.4

119

.43%

2.16

/m

l1.

74/m

l1.

83/m

l1.

83/m

l1.

83/m

lH

380

508

173

502

Alz

adA

lben

daz

ole

IP−4

00m

gTa

b1

14.8

011

.87

19.8

1%14

.80

11.8

712

.00

2.56

12.0

0H

112

240

532

Enp

ril

10m

gEn

alap

ril

Tab

1054

.86

49.3

710

.00%

5.49

4.94

2.18

2.18

L11

224

053

3En

pri

l5

mg

Enal

apri

lTa

b10

30.6

027

.54

10.0

0%3.

062.

751.

201.

20L

118

154

269

544

Lozi

tan

50m

gLo

sart

enTa

b10

46.4

232

.49

30.0

0%4.

643.

253.

903.

903.

90H

332

209

559

Nos

ocef

250

mg

Cef

tria

xon

eIn

j1

vial

47.4

837

.98

20.0

0%47

.48

37.9

848

.80

48.8

0H

322

344

205

565

O-P

ower

cef

100

mg

Cefi

xim

eD

TTa

b10

137.

1510

9.72

20.0

0%13

.72

10.9

727

.00

27.0

027

.00

H

322

205

566

O-P

ower

cef

200

mg

Cefi

xim

eTa

b4

100.

2380

.18

20.0

0%25

.06

20.0

549

.00

49.0

0H

322

205

567

O-P

ower

cef

DS

Cefi

xim

e50

mg/

5m

lLi

qu

id30

ml

63.3

050

.64

20.0

0%2.

11/m

l1.

69/m

l3.

27/m

l3.

27/m

lH

207

209

292

573

Pyre

xon

650

mg

Para

ceta

mol

-IP

-DT

Tab

69.

598.

6310

.00%

1.60

1.44

1.35

1.35

1.35

L

230

Tabl

eA

.1(C

onti

nu

ed)

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

7462

128

857

4R

ESEC

Om

epra

zole

–IP

Cap

1046

.95

37.5

620

.00%

4.70

3.76

3.98

3.95

3.98

H

195

602

Bec

laso

ne

–C

15gm

Top

ical

Ster

oid

sC

ream

15gm

22.9

014

.80

35.3

7%1.

53/g

m0.

99/g

m1.

53/g

mH

195

603

Bec

laso

ne

–C

5gm

Top

ical

Ster

oid

sC

ream

5gm

11.7

58.

6026

.81%

2.35

/gm

1.72

/gm

2.35

/gm

H

195

604

BEC

LASO

NE

–G

M15

gmTo

pic

alSt

eroi

ds

Cre

am15

gm24

.90

16.9

032

.13%

1.66

/gm

1.13

/gm

1.66

/gm

H

195

605

Bec

laso

ne

–G

M5

gmTo

pic

alSt

eroi

ds

Cre

am5

gm13

.90

9.60

30.9

4%2.

78/g

m1.

92/g

m2.

78/g

mH

219

608

Cip

robi

otic

–25

0A

nti

-B

acte

rial

Tab

1030

.66

11.6

062

.17%

3.07

1.16

2.88

H

219

609

Cip

robi

otic

–50

0A

nti

-B

acte

rial

Tab

1059

.42

20.4

065

.67%

5.94

2.04

5.87

H

220

610

Cip

robi

otic

–T

N–

250

An

ti-

Bac

teri

alTa

b10

34.6

422

.20

35.9

1%3.

462.

222.

99H

220

611

Cip

robi

otic

–T

N–

500

An

ti-

Bac

teri

alTa

b10

67.9

439

.10

42.4

5%6.

793.

915.

99H

297

181

671

Ran

oxyl

Cap

s25

0m

gA

mox

icil

lin

Cap

1042

.00

37.8

010

.00%

4.20

3.78

3.00

3.00

L

231

297

181

672

Ran

oxyl

Cap

s50

0m

gA

mox

icil

lin

Cap

1067

.20

60.4

810

.00%

6.72

6.05

5.30

5.30

L

297

181

675

Ran

oxyl

Syru

p60

ml.

Am

oxic

illi

n12

5m

g/5

ml

Dry

syru

p60

ml

29.4

026

.46

10.0

0%0.

49/m

l0.

44/m

l0.

42/m

l0.

42/m

lL

155

149

240

688

Invo

ril

5mg

Enal

apri

l5

mg

Tab

1023

.73

18.9

820

.02%

2.38

1.90

1.88

1.88

1.88

L38

017

370

2Lu

pib

end

400

An

thel

min

tics

Tab

50×

162

6.76

575.

008.

26%

12.5

411

.50

12.0

012

.00

H38

227

070

3Lu

pim

ebA

nth

elm

inti

csTa

b20

×6

240.

2621

9.20

8.76

%2.

001.

101.

921.

92H

7628

871

0Lu

pom

e-D

An

tip

epti

cU

lcer

ants

Cap

20×

1094

0.14

835.

6011

.12%

4.70

4.18

4.18

4.18

E

134

178

711

Defi

din

5m

gA

nti

hyp

erte

nsi

ves

Tab

1067

8.99

600.

6011

.55%

2.26

2.00

2.17

2.17

H38

017

371

6Lu

pib

end

10m

lA

nth

elm

inti

csSy

rup

10m

l21

.94

18.8

014

.30%

2.19

/m

l1.

88/m

l2.

102.

10/m

lH

354

285

723

Eufo

x20

0A

nti

biot

ics

Tab

10×

1088

7.91

731.

2017

.65%

8.88

7.31

7.31

7.31

E35

628

672

5Eu

fox-

Tz

An

tibi

otic

sTa

b10

×10

1044

.60

835.

6020

.01%

10.4

58.

368.

368.

36E

509

275

742

Lup

igyl

Gel

An

thel

min

tics

Gel

30gm

28.2

020

.35

27.8

5%0.

94/gm

0.68

/gm

1.35

/gm

1.35

/gm

H23

228

174

8Lu

pis

uli

de

Gel

Pain

Man

agem

ent

Gel

30gm

25.0

716

.70

33.3

9%0.

84/gm

0.56

/gm

1.20

/gm

1.20

/gm

H

232

281

753

Lup

isu

lid

ePa

inM

anag

emen

tTa

b5

×5

×10

626.

7639

1.75

37.5

0%2.

501.

562.

402.

40H

7629

176

2Lu

pip

an40

An

tip

epti

cU

lcer

ants

Tab

10×

1062

6.76

313.

4050

.00%

6.27

3.13

6.00

6.00

H

320

354

204

768

Rof

ex50

0m

gC

aps

An

hyd

rou

sC

eph

alax

inC

ap10

×10

118.

1810

5.00

11.1

5%1.

181.

0510

.57

11.8

210

.57

H

320

354

204

771

Cep

hal

axin

Cep

hal

axin

Cap

20×

1062

.66

60.0

04.

25%

0.31

0.30

5.94

6.27

5.94

H28

178

6N

icip

An

alge

sics

/A

nti

pyr

etic

s/A

nti

-in

flam

mat

ory

Tab

10’s

25.0

021

.00

16.0

0%2.

502.

102.

50H

212

787

Cet

cip

An

tial

lerg

icTa

b10

’s33

.65

25.0

025

.71%

3.37

2.50

2.75

H

232

Tabl

eA

.1(C

onti

nu

ed)

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

287

788

Om

ecip

10A

nta

cid

Cap

10’s

24.0

019

.50

18.7

5%2.

401.

952.

40H

287

789

Om

ecip

20A

nta

cid

Cap

15’s

58.5

046

.00

21.3

7%3.

903.

073.

90H

281

790

Nod

ard

An

alge

sics

/A

nti

pyr

etic

s/A

nti

-in

flam

mat

ory

Tab

10’s

25.0

021

.00

16.0

0%2.

502.

102.

50H

232

282

792

Nic

iflex

-TA

nal

gesi

cs/

An

tip

yret

ics/

An

ti-

infl

amm

ator

y

Tab

10’s

55.0

040

.00

27.2

7%5.

504.

005.

505.

50H

189

236

793

Vom

isto

p10

DT

An

tiem

etic

s/A

nti

nau

sean

tsTa

b10

’s24

.00

16.0

033

.33%

2.40

1.60

2.40

2.40

H

408

330

794

Bro

mex

An

tiC

ough

&C

old

Prep

arat

ion

s

Liq

uid

100

ml

27.0

022

.00

18.5

2%0.

27/m

l0.

22/m

l0.

27/m

l0.

27/m

lH

308

187

796

Meg

asyn

250

An

tibi

otic

sC

ap10

’s30

.00

24.0

020

.00%

3.00

2.40

3.00

3.00

H

241

230

798

Ver

ub

Pain

reli

evin

goi

ntm

ent

Gel

30gm

37.0

030

.00

18.9

2%1.

23/g

m1.

00/g

m1.

23/g

m1.

23/g

mH

313

799

Bu

rnh

eal

An

tise

pti

cPo

wd

er10

gm21

.00

16.0

023

.81%

2.10

/gm

1.60

/gm

2.10

/gm

H

233

293

800

Para

cod

An

alge

sics

/A

nti

pyr

etic

s/A

nti

-in

flam

mat

ory

Tab

10’s

31.0

025

.00

19.3

5%3.

102.

503.

10H

382

264

801

Levo

mol

50A

nth

elm

inti

csTa

b1’

s7.

756.

0022

.58%

7.75

6.00

7.75

7.75

H38

226

480

2Le

vom

ol15

0A

nth

elm

inti

csTa

b1’

s15

.70

13.5

014

.01%

15.7

013

.50

15.7

015

.70

H23

880

3V

omin

ate

An

tiem

etic

s/A

nti

nau

sean

tsTa

b10

’s19

.50

15.0

023

.08%

1.95

1.50

1.95

H

344

804

Q-G

at20

0A

nti

biot

ics

&A

nti

bact

eria

lsTa

b5’

s40

.00

33.0

017

.50%

8.00

6.60

8.00

H

242

383

806

Pow

erge

lPa

inre

liev

ing

oin

tmen

tG

el30

gm37

.00

30.0

018

.92%

1.23

/gm

1.00

/gm

1.23

/gm

1.23

/gm

H

196

296

807

Phen

oton

e30

An

tiep

ilep

tic

dru

gsTa

b10

’s7.

406.

0018

.92%

0.74

0.60

0.74

0.74

H

196

296

808

Phen

oton

e60

An

tiep

ilep

tic

dru

gsTa

b10

’s10

.20

9.00

11.7

6%1.

020.

901.

021.

02H

346

809

Feri

cip

Vit

amin

sSu

pp

lem

ents

Cap

10’s

73.3

455

.00

25.0

1%7.

335.

504.

50H

173

810

Alf

aric

h0.

25V

itam

ins

Sup

ple

men

tsC

ap10

’s65

.00

50.0

023

.08%

6.50

5.00

5.00

E

518

195

811

Bec

der

mTo

pic

alp

rep

arat

ion

sC

ream

15gm

18.0

015

.00

16.6

7%1.

20/g

m1.

00/g

m1.

20/g

m1.

20/g

mH

408

330

813

Bro

mex

An

tiC

ough

&C

old

Prep

arat

ion

s

Cre

am10

’s12

.00

9.00

25.0

0%1.

200.

901.

201.

20H

519

814

Clo

der

mA

nti

fun

gal

crea

mC

ream

15gm

28.0

024

.00

14.2

9%1.

871.

602.

13/g

mH

409

331

815

Cof

dex

Fort

eA

nti

Cou

gh&

Col

dPr

epar

atio

ns

Liq

uid

100

ml

35.0

029

.00

17.1

4%0.

35/m

l0.

29/m

l0.

35/m

l0.

35/m

lH

234

Tabl

eA

.1(C

onti

nu

ed)

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

335

816

Rid

cof

An

tiC

ough

&C

old

Prep

arat

ion

s

Liq

uid

60m

l20

.00

17.0

015

.00%

0.33

/ml

0.28

/ml

0.33

/ml

H

409

331

817

Cof

dex

Plu

sA

nti

Cou

gh&

Col

dPr

epar

atio

ns

Liq

uid

60m

l27

.00

23.0

014

.81%

0.27

/ml

0.23

/ml

0.27

/ml

0.27

/ml

H

332

818

Dex

cof

An

tiC

ough

&C

old

Prep

arat

ion

s

Liq

uid

100

ml

30.0

027

.00

10.0

0%0.

30/m

l0.

27/m

l0.

30/m

lH

236

299

819

Dol

ocip

DT

An

alge

sics

/A

nti

pyr

etic

s/A

nti

-in

flam

mat

ory

Tab

10’s

44.5

025

.00

43.8

2%4.

452.

503.

003.

00H

7325

582

3H

elip

acK

itA

nta

cid

Tab

6’s

Kit

25.2

020

.00

20.6

3%4.

203.

334.

204.

20H

228

254

824

Ost

eoci

pA

nal

gesi

cs/

An

tip

yret

ics/

An

ti-

infl

amm

ator

y

Tab

10’s

150.

0010

0.00

33.3

3%15

.00

10.0

015

.00

15.0

0h

411

333

825

Lexc

ofA

nti

Cou

gh&

Col

dPr

epar

atio

ns

Liq

uid

50m

l26

.00

23.0

011

.54%

0.52

/ml

0.46

/ml

0.52

/ml

0.52

/ml

H

235

428

349

827

Max

ifer

onso

ftV

itam

ins/

Nu

trit

ion

alSu

pp

lem

ents

Cap

10’s

27.0

023

.00

14.8

1%2.

702.

302.

702.

70H

7327

882

8M

osap

id5

An

taci

dTa

b10

’s27

.00

20.0

025

.93%

2.70

2.00

2.70

2.70

H31

883

1To

scof

An

tiC

ough

&C

old

Prep

arat

ion

s

Liq

uid

100

ml

30.0

024

.00

20.0

0%0.

30/m

l0.

24/m

l0.

30/m

lH

8237

183

2U

riso

da

Syst

emic

Alk

aliz

erG

ran

ule

s4

gm8.

506.

0029

.41%

2.13

/gm

1.50

/gm

2.13

/gm

2.13

/gm

H

275

833

Vom

inor

mA

nti

emet

ics/

An

tin

ause

ants

Inj

2m

l6.

004.

0033

.33%

3.00

2.00

3.00

H

178

229

834

Zep

ose

An

tid

epre

ssan

tIn

j2

ml

12.0

06.

0050

.00%

6.00

/ml

3.00

/ml

6.00

/ml

6.00

/ml

H30

232

618

483

5C

lava

m37

5m

gA

mox

icil

lin

+C

lavu

lan

ate

Pota

ssiu

m

Tab

10’s

296.

4019

7.08

33.5

1%29

.64

19.9

128

.50

28.5

028

.50

H

302

326

184

836

Cla

vam

625

mg

Am

oxic

illi

n+

Cla

vula

nat

ePo

tass

ium

Tab

10’s

379.

6020

7.48

45.3

4%37

.96

20.7

519

.95

36.5

019

.95

H

302

326

184

837

Cla

vam

Am

oxic

illi

nA

nd

Cla

vula

nat

e

Dry

syru

p30

ml

72.8

048

.78

33.0

0%2.

43/m

l1.

63/m

l2.

50/m

l2.

33/m

l2.

50/m

lH

302

326

184

839

Cla

vam

1000

mg

Am

oxic

illi

n+

Cla

vula

nat

ePo

tass

ium

Tab

10’s

483.

6031

1.48

35.5

9%48

.36

31.1

529

.95

46.5

029

.95

H

302

184

840

Cla

vam

DT

Am

oxic

illi

n+

Cla

vula

nat

ePo

tass

ium

Tab

10’s

132.

6082

.68

37.6

5%13

.26

8.27

12.7

512

.75

H

1127

845

Gem

fos

Ris

edro

nat

eSo

diu

mTa

b4’

s20

8.00

124.

8040

.00%

52.0

031

.20

50.0

0H

330

351

209

847

Tazi

d25

0m

gC

efta

zid

ime

Inj

Via

l86

.32

78.0

09.

64%

86.3

278

.00

85.0

075

.00

85.0

0H

236

Tabl

eA

.1(C

onti

nu

ed)

CIM

SD

TID

RO

rigi

nal

Nam

eo

fth

efo

rmu

lati

on

and

stre

ngt

h

Th

erap

euti

cca

tego

ry/

Co

mp

osi

tio

n

Cla

imed

pri

ces

Mar

ket

pri

ces

Pag

e/re

fere

nce

S.N

o.

Pac

kSi

zeO

ldp

rice

(Rs.

)

New

pri

ce(R

s.)

Red

uct

ion

%ag

eO

ldp

rice

per

un

it

New

pri

cep

eru

nit

CIM

SD

TID

RSt

atu

s

330

351

209

848

Tazi

d50

0m

gC

efta

zid

ime

Inj

Via

l16

1.20

145.

609.

68%

161.

2014

5.60

140.

0016

2.00

140.

00M

330

351

209

849

Tazi

d10

00m

gC

efta

zid

ime

Inj

Via

l28

0.80

192.

4031

.48%

280.

8019

2.40

270.

0018

5.00

270.

00H

382

850

Zoce

f25

0m

gC

efu

roxi

me

Sod

ium

Inj

Via

l58

.76

46.8

020

.35%

58.7

646

.80

56.5

0H

336

382

211

851

Zoce

f75

0m

gC

efu

roxi

me

Sod

ium

Inj

Via

l11

8.56

99.8

415

.79%

118.

5699

.84

99.8

411

4.00

99.8

4M

382

852

Zoce

f1.

5gm

Cef

uro

xim

eSo

diu

mIn

jV

ial

225.

6818

7.20

17.0

5%22

5.68

187.

2021

7.00

H

382

853

Zoce

f12

5m

gC

efu

roxi

me

Axe

til

Tab

10’s

161.

2013

5.20

16.1

3%16

.12

13.5

215

.50

H

382

854

Zoce

f25

0m

gC

efu

roxi

me

Axe

til

Tab

10’s

338.

0020

6.96

38.7

7%33

.80

20.7

032

.50

H

382

855

Zoce

f50

0m

gC

efu

roxi

me

Axe

til

Tab

10’s

676.

0039

5.20

41.5

4%67

.60

39.5

265

.00

H

367

209

859

Cef

xo1

gmC

eftr

iaxo

ne

Inj

Via

l98

.00

82.0

016

.32%

98.0

082

.00

75.0

075

.00

L36

720

986

0C

efxo

250

mg

Cef

tria

xon

eIn

jIn

jV

ial

43.0

035

.80

16.7

4%43

.00

35.8

030

.00

30.0

0L

237

367

209

861

Cef

xo50

0m

gC

eftr

iaxo

ne

Inj

Inj

Via

l58

.00

48.3

016

.72%

58.0

048

.30

50.0

050

.00

H47

621

286

4O

nce

tC

etir

izin

eD

ihyd

roch

lori

de

Tab

10’s

25.0

015

.00

40.0

0%2.

501.

501.

001.

00L

382

507

270

876

Hel

min

tol

100

mg

Meb

end

azol

eTa

b6’

s6.

955.

8016

.55%

1.16

0.97

0.99

1.16

0.99

H24

528

187

8N

imsa

idN

imes

uli

de

Tab

10’s

24.0

020

.00

16.6

7%2.

402.

001.

871.

87L

697

313

882

Vig

reks

100

mg

Sild

enafi

lC

itra

teTa

b4’

s10

8.00

90.0

016

.67%

27.0

022

.50

25.0

025

.00

H

697

313

883

Vig

reks

50m

gSi

lden

afil

Cit

rate

Tab

4’s

72.0

060

.00

16.6

7%18

.00

15.0

014

.90

14.9

0L

Not

e:C

IMS,

DT

(Dru

gTo

day

),an

dID

Rar

eco

nsi

der

edto

refl

ect

the

mar

ket

pri

ces.

Th

ele

tter

inth

ela

stco

lum

nre

pre

sen

tsth

est

atu

sof

the

mar

ket

pri

cere

lati

veto

the

clai

med

pri

cere

du

ctio

n.

H=

the

mar

ket

pri

ceis

hig

her

than

the

clai

med

pri

ce;

L=

the

mar

ket

pri

ceis

low

erth

anth

ecl

aim

edp

rice

;E

=th

em

arke

tp

rice

iseq

ual

toth

ecl

aim

edp

rice

;an

dM

=th

em

arke

tp

rice

ism

ixed

,wh

ich

mea

ns

atle

ast

inon

eof

the

refe

ren

cebo

oks

the

pri

ceis

hig

her

wh

ile

inth

eot

her

book

sth

ep

rice

islo

wer

than

the

clai

med

pri

ce.

Sour

ce:A

uth

orca

lcu

lati

ons

base

don

Gov

ern

men

tof

Ind

ia(2

006h

),C

IMS

(200

7),D

rug

Tod

ay(2

007)

,an

dID

R(2

008)

.

Appendix B

238

239

Ex

amin

atio

no

fch

ange

sto

dru

gp

rice

s

Tabl

eB

.1Pr

ice

chan

ges

tod

rugs

for

card

iova

scu

lar

dis

ease

s

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Car

bop

rost

Trom

eth

amin

ePr

osto

din

Inj

250

mcg

/ml

1m

lU

teri

ne

stim

ula

nts

Ast

raZe

nec

a−2

.74

24.3

1

Car

bop

rost

Trom

eth

amin

eD

evip

rost

Inj

250

mcg

/ml

1m

lU

teri

ne

stim

ula

nts

DR

L12

.97

Sild

enafi

lC

itra

teA

lsig

raTa

b25

mg

4U

teri

ne

stim

ula

nts

Ale

mbi

c0.

00

Sild

enafi

lC

itra

teA

lsig

raTa

b50

mg

4U

teri

ne

stim

ula

nts

Ale

mbi

c0.

00

Bis

opro

lol

Con

cor

Tab

5m

g10

An

ti-a

ngi

nal

sM

erck

−5.5

59.

34A

ten

olol

+N

ifed

ipin

eye

sC

ard

ule

sPl

us

10m

gTa

b50

mg

+10

mg

10A

nti

-an

gin

als

Nic

hol

asPi

ram

al3.

7440

.00

Ate

nol

ol+

Nif

edip

ine

yes

Car

du

les

Plu

s20

mg

Tab

50m

g+

20m

g10

An

ti-a

ngi

nal

sN

ich

olas

Pira

mal

37.5

9

Nif

edap

ine

yes

Cad

ule

sC

ap10

mg

10A

nti

-an

gin

als

Nic

hol

asPi

ram

al43

.18

Nif

edap

ine

yes

Cad

ule

sC

ap10

mg

(Ret

ard

)10

An

ti-a

ngi

nal

sN

ich

olas

Pira

mal

62.8

0

Nif

edap

ine

yes

Cad

ule

sC

ap20

mg

(Ret

ard

)10

An

ti-a

ngi

nal

sN

ich

olas

Pira

mal

35.4

8

Nif

edip

ine

yes

Dep

inC

ap5

mg

50×

3A

nti

-an

gin

als

Zyd

us

Cad

ila

6.24

0.00

Nif

edip

ine

yes

Dep

inC

ap10

mg

30A

nti

-an

gin

als

Zyd

us

Cad

ila

0.00

Nif

edip

ine

yes

Dep

inC

ap20

mg

(Ret

ard

)30

An

ti-a

ngi

nal

sZy

du

sC

adil

a0.

00

240

Tabl

eB

.1(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Ind

apam

ide

Lorv

asTa

b2.

5m

g10

An

ti-h

ypot

ensi

ves

Torr

ent

6.78

0.00

Met

opro

lol+

Hyd

roch

loro

thia

zid

eSe

lop

res

Tab

100

mg

+12

.5m

g10

An

ti-H

yper

ten

sive

sA

stra

Zen

eca

0.00

0.00

Ch

lon

idin

e+

Hyd

roch

loro

thia

zid

eye

sA

rkam

in-H

Tab

100

mcg

+20

mg

10A

nti

-Hyp

erte

nsi

ves

Un

isea

rch

2.05

17.8

5

Ch

lon

idin

eye

sA

rkam

inTa

b10

0m

cg10

An

ti-H

yper

ten

sive

sU

nis

earc

h18

.46

Enal

apri

lm

alea

teye

sEn

ace

Tab

2.5

mg

10A

nti

-Hyp

erte

nsi

ves

Nic

hol

asPi

ram

al4.

5218

.80

Enal

apri

lm

alea

teye

sEn

ace

Tab

5m

g10

An

ti-H

yper

ten

sive

sN

ich

olas

Pira

mal

20.2

3

Enal

apri

lm

alea

teye

sEn

ace

Tab

10m

g10

An

ti-H

yper

ten

sive

sN

ich

olas

Pira

mal

6.90

Enal

apri

lm

alea

te+

Hyd

roch

loro

thia

zid

eye

sEn

ace-

DTa

b10

mg

+25

mg

10A

nti

-Hyp

erte

nsi

ves

Nic

hol

asPi

ram

al5.

8715

.64

Res

erp

ine

+D

ihyd

rall

azin

e+

Hyd

roch

loro

thia

zid

e

Ad

elp

han

e-Es

idre

xTa

b0.

1m

g+

10m

g+

10m

g10

An

ti-H

yper

ten

sive

sN

ovar

tis

7.00

10.1

4

Res

erp

ine

+D

ihyd

rall

azin

eA

del

ph

ane

Tab

0.1

mg

+10

mg

10A

nti

-Hyp

erte

nsi

ves

Nov

arti

s10

.14

Ram

ipri

lC

ard

ace

Tab

1.25

mg

10C

ard

iac

Dis

ord

ers

San

ofi-

Ave

nti

s2.

130.

00

Ram

ipri

lC

ard

ace

Tab

2.5

mg

10C

ard

iac

Dis

ord

ers

San

ofi-

Ave

nti

s1.

43

Ram

ipri

lC

ard

ace

Tab

5m

g10

Car

dia

cD

isor

der

sSa

nofi

-A

ven

tis

5.00

Ram

ipri

lC

ard

ace

Tab

10m

g10

Car

dia

cD

isor

der

sSa

nofi

-A

ven

tis

0.00

241

Ram

ipri

l+

Hyd

roch

loro

thia

zid

eC

ard

ace

–H

Tab

2.5

mg

+12

.5m

g10

Car

dia

cD

isor

der

sSa

nofi

-A

ven

tis

4.76

Dig

oxin

yes

Car

dio

xin

Tab

0.25

mg

10C

ard

iac

Dis

ord

ers

Nov

arti

s11

.28

0.00

Dig

oxin

yes

Lan

oxin

Tab

0.25

mg

10C

ard

iac

Dis

ord

ers

GSK

16.6

417

.63

Ate

nol

ol+

Nif

edip

ine

yes

Ten

ofed

Cap

50m

g+

20m

g10

Peri

ph

eral

Vas

odil

ator

sIP

CA

−0.3

56.

89

Ate

nol

olTe

nol

olTa

b25

mg

14Pe

rip

her

alV

asod

ilat

ors

IPC

A7.

517.

84

Ate

nol

olye

sTe

nol

olTa

b50

mg

14Pe

rip

her

alV

asod

ilat

ors

IPC

A8.

73

Ate

nol

olye

sTe

nol

olTa

b10

0m

g14

Peri

ph

eral

Vas

odil

ator

sIP

CA

0.00

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

242

Tabl

eB

.2Pr

ice

chan

ges

tod

rugs

for

cen

tral

ner

vou

ssy

stem

dis

ord

ers

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Para

ceta

mol

+C

affe

ine

+C

adei

ne

yes

Zim

algi

nC

ap50

0m

g+

15m

g+

5m

g10

Mas

tce

llst

abli

zer

Shre

ya7.

480.

08

Asp

irin

+C

alca

rbor

ae+

An

hyd

rou

sci

tric

acid

yes

Dis

pri

nTa

b35

0m

g+

105

mg

+35

mg

12×

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Rec

kitt

Ben

ckis

er−0

.26

0.00

Car

bam

azep

ine

yes

yes

Maz

etol

Tab

100

mg

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Nic

hol

asPi

ram

al−1

.36

1.93

Car

bam

azep

ine

yes

yes

Maz

etol

Tab

200

mg

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Nic

hol

asPi

ram

al1.

87

Car

bam

azep

ine

yes

Maz

etol

Tab

400

mg

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Nic

hol

asPi

ram

al6.

83

Car

bam

azep

ine

yes

yes

Maz

etol

–SR

Tab

200

mg

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Nic

hol

asPi

ram

al2.

43

Car

bam

azep

ine

yes

Maz

etol

–SR

Tab

400

mg

10A

nal

gesi

csan

dA

nti

pyr

etic

s

Nic

hol

asPi

ram

al2.

25

Met

oclo

pro

mid

eye

sR

egla

nTa

b10

mg

10A

nti

emet

ics

and

An

tin

au-

sean

ts

CFL

Phar

ma

3.57

31.2

3

Met

oclo

pro

mid

eye

sR

egla

nSy

rup

5m

g/5

ml

30m

lA

nti

emet

ics

and

An

tin

au-

sean

ts

CFL

Phar

ma

29.8

2

243

Met

oclo

pro

mid

eR

egla

nIn

j10

mg/

ml

2m

lA

nti

emet

ics

and

An

tin

ause

ants

CFL

Phar

ma

33.3

3

Met

oclo

pro

mid

eR

egla

nIn

j10

mg/

ml

10m

lA

nti

emet

ics

and

An

tin

ause

ants

CFL

Phar

ma

29.6

3

Met

oclo

pro

mid

eye

sR

egla

nTa

b10

mg

10In

test

inal

mot

ilit

y/A

lim

enta

rysy

stem

CFL

Phar

ma

0.00

Met

oclo

pro

mid

eye

sR

egla

nSy

rup

5m

g/5

ml

30m

lIn

test

inal

mot

ilit

y/A

lim

enta

rysy

stem

CFL

Phar

ma

0.00

Met

oclo

pro

mid

eR

egla

nIn

j10

mg/

ml

2m

lIn

test

inal

mot

ilit

y/A

lim

enta

rysy

stem

CFL

Phar

ma

0.00

Met

oclo

pro

mid

eR

egla

nIn

j10

mg/

ml

10m

lIn

test

inal

mot

ilit

y/A

lim

enta

rysy

stem

CFL

Phar

ma

0.00

Imip

ram

ine

yes

An

tid

epTa

b25

mg

10A

nti

dep

ress

ants

Torr

ent

2.12

0.00

Imip

ram

ine

yes

An

tid

epTa

b75

mg

10A

nti

dep

ress

ants

Torr

ent

0.00

Lith

ium

Car

bon

ate

Lica

b/X

LTa

b30

0m

g10

An

tid

epre

ssan

tsTo

rren

t−1

.04

0.00

Lith

ium

Car

bon

ate

Lica

bTa

b40

0m

g10

An

tid

epre

ssan

tsTo

rren

t0.

00Lo

raze

pam

Larp

ose

Tab

1m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sC

ipla

−0.4

213

.33

Lora

zep

amLa

rpos

eTa

b2

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

Cip

la13

.90

Trifl

uop

eraz

ine

+Tr

ihex

yph

enid

ylye

sTr

inic

alm

Plu

sTa

b5

mg

+2

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

Torr

ent

−0.1

30.

00

Trifl

uop

eraz

ine

+Tr

ihex

yph

enid

yl+

Ch

lorp

rom

azin

e

yes

yes

Trin

ical

mFo

rte

Tab

5m

g+

2m

g+

50m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sTo

rren

t0.

00

Trifl

uop

eraz

ine

yes

Trin

ical

mTa

b5

mg

10A

nti

emet

ics

and

An

tin

ause

ants

Torr

ent

0.00

Clo

zap

ine

Sizo

pin

Tab

25m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sSu

nPh

arm

a0.

008.

57

244

Tabl

eB

.2(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Clo

zap

ine

Sizo

pin

Tab

100

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

Sun

Phar

ma

3.24

Hal

oper

idol

yes

Sere

nac

eTa

b1.

5m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sR

PGPh

arm

a0.

0023

.77

Hal

oper

idol

yes

Sere

nac

eTa

b5

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

RPG

Phar

ma

23.5

3

Hal

oper

idol

yes

Sere

nac

eTa

b10

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

RPG

Phar

ma

23.7

7

Hal

oper

idol

Sere

nac

eTa

b20

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

RPG

Phar

ma

10.2

1

Hal

oper

idol

Sere

nac

eLi

qu

id2

mg/

1m

l15

ml

Sed

ativ

esan

dTr

anq

uil

iser

sR

PGPh

arm

a50

.38

Hal

oper

idol

yes

Sere

nac

eIn

j5

mg/

ml

1m

lSe

dat

ives

and

Tran

qu

ilis

ers

RPG

Phar

ma

42.7

2

Clo

zap

ine

Loza

pin

Tab

25m

g10

An

tiem

etic

san

dA

nti

nau

sean

ts

Torr

ent

1.76

0.00

Clo

zap

ine

Loza

pin

Tab

100

mg

10A

nti

emet

ics

and

An

tin

ause

ants

Torr

ent

0.00

Dia

zep

amye

sPa

xum

Tab

5m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sEa

stIn

dia

2.40

37.4

4

Dia

zep

amye

sPa

xum

Inj

5m

g/m

l2

ml

Sed

ativ

esan

dTr

anq

uil

iser

sEa

stIn

dia

38.5

4

Dia

zep

amEl

cion

CR

Cap

10m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sR

anba

xy4.

130.

00

245

Lora

zep

amA

tiva

nTa

b1

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

Wye

th5.

660.

00

Lora

zep

amA

tiva

nTa

b2

mg

10Se

dat

ives

and

Tran

qu

ilis

ers

Wye

th0.

00

Flu

ph

enaz

ine

An

aten

sol

Inj.

Inj

25m

g/m

l1

ml

vial

Sed

ativ

esan

dTr

anq

uil

iser

sN

ich

olas

Pira

mal

12.9

90.

00

Flu

ph

enaz

ine

An

aten

sol

Inj.

Tab

1m

g10

Sed

ativ

esan

dTr

anq

uil

iser

sN

ich

olas

Pira

mal

0.00

Phen

obar

bito

ne

yes

Gar

den

alTa

b30

mg

10H

ypn

otic

sN

ich

olas

Pira

mal

0.00

40.1

7

Phen

obar

bito

ne

yes

Gar

den

alTa

b60

mg

10H

ypn

otic

sN

ich

olas

Pira

mal

38.4

0

Phen

obar

bito

ne

Gar

den

alSy

rup

20m

g/5

ml

60m

lH

ypn

otic

sN

ich

olas

Pira

mal

23.3

7

Phen

ytoi

n+

Phen

obar

bito

ne

yes

Gar

oin

Tab

100

mg

+50

mg

10A

nti

con

vuls

ants

Nic

hol

asPi

ram

al7.

0031

.54

Phen

ytoi

nSo

diu

mD

ilan

tin

Kap

seal

s10

0m

g10

0A

nti

con

vuls

ants

Pfize

r0.

0024

.04

Phen

ytoi

nSo

diu

mD

ilan

tin

Kap

seal

s25

mg

100

An

tico

nvu

lsan

tsPfi

zer

26.0

1Ph

enyt

oin

Sod

ium

yes

Dil

anti

nSy

rup

25m

g/m

l10

0m

lA

nti

con

vuls

ants

Pfize

r21

.28

Phen

ytoi

nSo

diu

m+

Eth

anol

yes

Dil

anti

nIn

j50

mg

+9.

5%v/

v2

ml

An

tico

nvu

lsan

tsPfi

zer

21.4

3

Phen

ytoi

n+

Phen

obar

bito

ne

Dil

anti

n–

PK

apse

als

100

mg

+32

mg

100

An

tico

nvu

lsan

tsPfi

zer

0.00

Phen

ytoi

nSo

diu

mye

sEp

soli

nTa

b10

0m

g10

0A

nti

con

vuls

ants

Cad

ila

4.21

0.00

Phen

ytoi

nSo

diu

mye

sEp

soli

nIn

j50

mg/

ml

50×

2m

lA

nti

con

vuls

ants

Cad

ila

0.00

Phen

ytoi

nSo

diu

mye

sEp

toin

Tab

50m

g50

An

tico

nvu

lsan

tsA

bbot

t8.

320.

00Ph

enyt

oin

Sod

ium

yes

Epto

inTa

b10

0m

g10

0A

nti

con

vuls

ants

Abb

ott

0.00

Phen

ytoi

nSo

diu

mEp

toin

Syru

p30

mg/

5m

l20

0m

lA

nti

con

vuls

ants

Abb

ott

0.00

Trih

exyp

hen

idyl

yes

Paci

tan

eTa

b2

mg

10N

euro

deg

ener

ativ

eD

isea

seW

yeth

6.70

0.00

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

246

Tabl

eB

.3Pr

ice

chan

ges

tod

rugs

for

infe

ctio

ns

and

infe

stat

ion

s

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Cef

tria

xon

eso

diu

mM

onoc

efIn

j12

5m

gV

ial

An

tibi

otic

sA

rist

o−2

.58

1.82

Cef

tria

xon

eso

diu

mye

sM

onoc

efIn

j25

0m

gV

ial

An

tibi

otic

sA

rist

o6.

76

Cef

tria

xon

eso

diu

mM

onoc

efIn

j50

0m

gV

ial

An

tibi

otic

sA

rist

o5.

24

Cef

tria

xon

eso

diu

mye

sM

onoc

efIn

j1

gmV

ial

An

tibi

otic

sA

rist

o2.

93

Cef

tria

xon

eso

diu

mM

onoc

efIn

j2

gmV

ial

An

tibi

otic

sA

rist

o2.

94

Cef

pod

oxim

ep

roxe

til

Mon

ocef

–O

Tab

100

mg

6A

nti

biot

ics

Ari

sto

−0.6

0

Cef

pod

oxim

ep

roxe

til

Mon

ocef

–O

Tab

200

mg

6A

nti

biot

ics

Ari

sto

−0.6

0

Cef

pod

oxim

ep

roxe

til

Mon

ocef

–O

Dry

syru

p50

mg/

5m

l30

ml

An

tibi

otic

sA

rist

o−1

.81

Cef

pod

oxim

ep

roxe

til

Mon

ocef

–O

Dry

syru

p10

0m

g/5

ml

30m

lA

nti

biot

ics

Ari

sto

−1.7

6

Cef

tria

xon

eso

diu

mye

sO

fram

axIn

j25

0m

gV

ial

An

tibi

otic

sR

anba

xy−0

.17

0.00

Cef

tria

xon

eso

diu

mO

fram

axIn

j50

0m

gV

ial

An

tibi

otic

sR

anba

xy0.

00

Cef

tria

xon

eso

diu

mye

sO

fram

axIn

j1

gmV

ial

An

tibi

otic

sR

anba

xy0.

00

Pen

icil

lin

-Gp

otye

sPe

nti

ds

–20

0Ta

b20

0,00

0i.

u6

An

tibi

otic

sN

ich

olas

Pira

mal

−0.0

56.

06

Pen

icil

lin

-Gp

otye

sPe

nti

ds

–40

0Ta

b40

0,00

0i.

u6

An

tibi

otic

sN

ich

olas

Pira

mal

6.25

247Pe

nic

illi

n-G

pot

yes

yes

Pen

tid

s–

600

Tab

600,

000

i.u

4A

nti

biot

ics

Nic

hol

asPi

ram

al6.

35

Ben

zath

ine

Pen

icil

lin

-Gye

sye

sPe

nco

mIn

j60

0,00

0i.

u5

vial

sA

nti

biot

ics

Ale

mbi

c0.

58−1

.27

Ben

zath

ine

Pen

icil

lin

-Gye

sye

sPe

nco

mIn

j1,

200,

000i

.u5

vial

sA

nti

biot

ics

Ale

mbi

c−1

.21

Ben

zath

ine

Pen

icil

lin

-Gye

sye

sPe

nid

ure

LA6

Inj

600,

000

i.u

Via

lA

nti

biot

ics

Wye

th0.

00

Ben

zath

ine

Pen

icil

lin

-Gye

sye

sPe

nid

ure

LA12

Inj

1,20

0,00

0i.

uV

ial

An

tibi

otic

sW

yeth

0.00

Ben

zath

ine

Pen

icil

lin

-Gye

sye

sPe

nid

ure

LA24

Inj

2,40

0,00

0i.

uV

ial

An

tibi

otic

sW

yeth

0.00

Eryt

hro

myc

inye

sye

sEr

yth

roci

nTa

b25

0m

g10

An

tibi

otic

sPfi

zer

8.57

−33.

62Er

yth

rom

ycin

yes

yes

Eryt

hro

cin

Tab

500

mg

10A

nti

biot

ics

Pfize

r−3

4.26

Eryt

hro

myc

inye

sye

sEl

toci

nTa

b25

0m

g10

An

tibi

otic

sIP

CA

3.03

−36.

08Er

yth

rom

ycin

yes

yes

Elto

cin

Tab

500

mg

10A

nti

biot

ics

IPC

A−5

8.39

Eryt

hro

myc

inye

sye

sEl

toci

nD

rysy

rup

125

mg/

5m

l30

ml

An

tibi

otic

sIP

CA

−34.

32C

efot

axim

eye

sye

sC

lafo

ran

Inj

250

mg

Via

lA

nti

biot

ics

San

ofi-

Ave

nti

s2.

220.

00

Cef

otax

ime

yes

yes

Cla

fora

nIn

j50

0m

gV

ial

An

tibi

otic

sSa

nofi

-A

ven

tis

0.00

Cef

otax

ime

yes

Cla

fora

nIn

j1

gmV

ial

An

tibi

otic

sSa

nofi

-A

ven

tis

0.00

Ch

lora

mp

hen

icol

yes

Rec

lor

Cap

250

mg

10A

nti

biot

ics

Nic

hol

asPi

ram

al0.

0015

.63

Ch

lora

mp

hen

icol

yes

Rec

lor

Cap

500

mg

6A

nti

biot

ics

Nic

hol

asPi

ram

al14

.86

Ch

lora

mp

hen

icol

yes

Ch

loro

myc

etin

Cap

500

mg

6A

nti

biot

ics

Pfize

r5.

7324

.14

Ch

lora

mp

hen

icol

yes

Ch

loro

myc

etin

Palm

itat

esu

sp12

5m

g/5

ml

60m

lA

nti

biot

ics

Pfize

r0.

00C

hlo

ram

ph

enic

olC

hlo

rom

ycet

inK

apse

al25

0m

g10

An

tibi

otic

sPfi

zer

24.2

5A

mox

icil

lin

+C

loxa

cill

inye

sye

sN

ovac

lox

Cap

s25

0m

g+

250

mg

9A

nti

biot

ics

Cip

la7.

19−5

2.65

Am

oxic

illi

n+

Clo

xaci

llin

yes

Nov

aclo

xP-

Tab

125

mg

+12

5m

g15

An

tibi

otic

sC

ipla

−51.

70

Am

oxic

illi

n+

Clo

xaci

llin

yes

Nov

aclo

x25

0In

j12

5m

g+

125

mg

Via

lA

nti

biot

ics

Cip

la0.

00

248

Tabl

eB

.3(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Am

oxic

illi

n+

Clo

xaci

llin

yes

yes

Nov

aclo

x50

0In

j25

0m

g+

250

mg

Via

lA

nti

biot

ics

Cip

la−1

.54

Am

oxic

illi

n+

Clo

xaci

llin

yes

yes

Nov

aclo

x10

00In

j50

0m

g+

500

mg

Via

lA

nti

biot

ics

Cip

la−1

.58

Am

oxic

illi

n+

Clo

xaci

llin

yes

Nov

aclo

xN

eon

ate

Inj

50m

g+

25m

g2

ml

vial

An

tibi

otic

sC

ipla

0.00

Am

oxic

illi

n+

Clo

xaci

llin

+La

ctic

Aci

dB

acil

lus

yes

yes

Nov

aclo

x–

LBC

ap25

0m

g+

250

mg

+60

mil

lion

cell

s

6A

nti

biot

ics

Cip

la−1

.58

Am

oxic

illi

nye

sye

sN

ovam

oxC

ap25

0m

g15

An

tibi

otic

sC

ipla

8.67

0.00

Am

oxic

illi

nye

sye

sN

ovam

oxC

ap50

0m

g6

An

tibi

otic

sC

ipla

0.00

Am

oxic

illi

nye

sye

sN

ovam

oxD

rysy

rup

125

mg/

5m

l30

ml

An

tibi

otic

sC

ipla

0.00

Am

oxic

illi

nye

sye

sN

ovam

oxD

rysy

rup

125

mg/

5m

l60

ml

An

tibi

otic

sC

ipla

0.00

Am

oxic

illi

nye

sN

ovam

ox(D

T)

Tab

125

mg

15A

nti

biot

ics

Cip

la0.

00

Am

oxic

illi

nye

sye

sN

ovam

ox(D

T)

Tab

250

mg

15A

nti

biot

ics

Cip

la0.

00

Am

pic

illi

nye

sye

sC

amp

icil

inC

ap25

0m

g10

An

tibi

otic

sC

adil

a10

.90

24.3

2A

mp

icil

lin

yes

yes

Cam

pic

ilin

Cap

500

mg

10A

nti

biot

ics

Cad

ila

−25.

22A

mp

icil

lin

yes

yes

Cam

pic

ilin

Dry

syru

p12

5m

g/5

ml

40m

lA

nti

biot

ics

Cad

ila

0.00

Am

pic

illi

nye

sye

sC

amp

icil

inD

rysy

rup

125

mg/

5m

l60

ml

An

tibi

otic

sC

adil

a7.

42A

mp

icil

lin

yes

Cam

pic

ilin

P-D

rop

s10

0m

g/m

l10

ml

An

tibi

otic

sC

adil

a0.

00A

mp

icil

lin

yes

Cam

pic

ilin

Inj

250

mg

Via

lA

nti

biot

ics

Cad

ila

0.00

Am

pic

illi

nye

sye

sC

amp

icil

inIn

j50

0m

gV

ial

An

tibi

otic

sC

adil

a0.

00A

mp

icil

lin

yes

yes

Bac

ipen

Cap

250

mg

4A

nti

biot

ics

Ale

mbi

c0.

00A

mp

icil

lin

yes

yes

Bac

ipen

Cap

500

mg

4A

nti

biot

ics

Ale

mbi

c0.

00

249

Am

pic

illi

nye

sye

sB

acip

enIn

j50

0m

gV

ial

An

tibi

otic

sA

lem

bic

0.00

Am

oxic

illi

n+

Clo

xaci

llin

yes

yes

Sup

rim

oxC

ap25

0m

g+

250

mg

15A

nti

biot

ics

Rex

cel/

Ran

baxy

3.89

−56.

36

Am

oxic

illi

n+

Clo

xaci

llin

yes

Sup

rim

oxP-

Tab

125

mg

+12

5m

g10

An

tibi

otic

sR

exce

l/R

anba

xy−5

1.48

Am

ph

oter

icin

Bye

sFu

ngi

zon

eIn

trav

enou

sIn

j50

mg

Via

lA

nti

fun

gals

Nic

hol

asPi

ram

al7.

500.

00

Clo

fazi

min

eye

sH

anse

pra

nC

ap50

mg

10A

nti

lep

roti

csN

ich

olas

Pira

mal

7.85

0.00

Clo

fazi

min

eye

sH

anse

pra

nC

ap10

0m

g10

An

tile

pro

tics

Nic

hol

asPi

ram

al0.

00

Meb

end

azol

eye

sM

ebex

Tab

100

mg

6A

nth

elm

inti

csan

dot

her

anti

-in

fest

ive

dru

gs

Cip

la4.

91

Meb

end

azol

eye

sM

ebex

Susp

100

mg/

5m

l30

ml

An

thel

min

tics

and

oth

eran

ti-i

nfe

stiv

ed

rugs

Cip

la6.

66

Meb

end

azol

eM

ebex

Gra

nn

ule

s20

0m

g/5

mg

5gm

Sach

ets

An

thel

min

tics

and

oth

eran

ti-i

nfe

stiv

ed

rugs

Cip

la7.

20

Meb

end

azol

e+

Pyra

nte

lPa

moa

te

yes

Meb

exPl

us

Tab

150

mg

+10

0m

g2

An

thel

min

tics

and

oth

eran

ti-i

nfe

stiv

ed

rugs

Cip

la0.

00−1

.66

Met

ron

idaz

ole

yes

yes

Flag

ylTa

b20

0m

g10

An

ti-

amoe

bics

,an

ti-g

iard

iasi

s

Nic

hol

asPi

ram

al2.

52−1

.92

Met

ron

idaz

ole

yes

yes

Flag

ylTa

b40

0m

g10

An

ti-

amoe

bics

,an

ti-g

iard

iasi

s

Nic

hol

asPi

ram

al−1

.74

250

Tabl

eB

.3(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Met

ron

idaz

ole

yes

Flag

ylSu

sp20

0m

g/5

ml

30m

lA

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Nic

hol

asPi

ram

al−5

.13

Met

ron

idaz

ole

yes

Flag

ylSu

sp20

0m

g/5

ml

60m

lA

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Nic

hol

asPi

ram

al−4

.56

Met

ron

idaz

ole

+Fu

razo

lid

one

yes

yes

Flag

yl–

FTa

b40

0m

g+

100

mg

10A

nti

-dia

rrh

orea

lsN

ich

olas

Pira

mal

3.55

Met

ron

idaz

ole

+Fu

razo

lid

one

yes

yes

Flag

yl–

FSu

sp10

0m

g+

30m

g/5

ml

60m

lA

nti

-dia

rrh

orea

lsN

ich

olas

Pira

mal

7.40

Met

ron

idaz

ole

+D

ilox

anid

eFu

roat

e

yes

yes

Flag

yl–

DF

Tab

400

mg

+50

0m

g15

An

ti-d

iarr

hor

eals

Nic

hol

asPi

ram

al−0

.09

Met

ron

idaz

ole

yes

yes

Ari

stog

ylTa

b20

0m

g10

An

ti-a

moe

bics

,an

ti-g

iard

iasi

sA

rist

o4.

74−1

.09

Met

ron

idaz

ole

yes

yes

Ari

stog

ylTa

b40

0m

g10

An

ti-a

moe

bics

,an

ti-g

iard

iasi

sA

rist

o−1

.27

Met

ron

idaz

ole

yes

Ari

stog

ylSu

sp10

0m

g/5

ml

60m

lA

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Ari

sto

−1.1

7

Met

ron

idaz

ole

+Fu

razo

lid

one

+Si

met

hic

one

yes

yes

Ari

stog

yl–

FTa

b40

0m

g+

100

mg

+50

mg

10A

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Ari

sto

0.00

Met

ron

idaz

ole

+Fu

razo

lid

one

yes

Ari

stog

yl–

FSu

sp10

0m

g+

30m

g/5

ml

60m

lA

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Ari

sto

−1.3

2

Met

ron

idaz

ole

+D

ilox

anid

eFu

roat

e+

Sim

eth

icon

e

yes

yes

Ari

stog

ylPl

us

Tab

400

mg

+50

0m

g+

100

mg

10A

nti

-am

oebi

cs,

anti

-gia

rdia

sis

Ari

sto

−1.1

7

Cip

rofl

oxac

inye

sye

sC

ipro

win

Tab

250

mg

10Q

uin

olon

esA

lem

bic

0.00

0.00

251

Cip

rofl

oxac

inye

sye

sC

ipro

win

Tab

500

mg

10Q

uin

olon

esA

lem

bic

0.00

Cip

rofl

oxac

inye

sC

ipro

win

Tab

750

mg

10Q

uin

olon

esA

lem

bic

0.00

Cip

rofl

oxac

inye

sC

ipro

win

Infu

sion

100

mg/

50m

l10

0m

lQ

uin

olon

esA

lem

bic

0.00

Cip

rofl

oxac

in+

Trin

idaz

ole

yes

yes

Cip

row

in–

TZ

–25

0Ta

b25

0m

g+

300

mg

10A

nti

-d

iarr

hor

eals

Ale

mbi

c0.

00

Cip

rofl

oxac

in+

Trin

idaz

ole

yes

Cip

row

in–

TZ

–50

0Ta

b50

0m

g+

600

mg

10A

nti

-d

iarr

hor

eals

Ale

mbi

c0.

00

Cip

rofl

oxac

in+

Ben

zalk

oniu

mch

lori

de

yes

yes

Cip

row

inE/

ED

rop

sD

rop

s3

mg

+0.

012%

v/v/

ml

5m

lA

nti

-in

fect

ive

pre

pA

lem

bic

0.00

Cip

rofl

oxac

inye

sC

iplo

xTa

b10

0m

g10

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la3.

38−0

.83

Cip

rofl

oxac

inye

sye

sC

iplo

xTa

b25

0m

g10

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la−0

.80

Cip

rofl

oxac

inye

sye

sC

iplo

xTa

b50

0m

g10

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la−0

.80

Cip

rofl

oxac

inye

sC

iplo

xTa

b75

0m

g10

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la−0

.80

Cip

rofl

oxac

inye

sC

iplo

xIn

fusi

onIn

fusi

on10

0m

g/50

ml

100

ml

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la0.

00

Cip

rofl

oxac

inye

sye

sC

iplo

x–

OD

Tab

500

mg

5Su

lph

onam

ides

and

oth

erB

act.

Cip

la0.

00

Cip

rofl

oxac

inye

sC

iplo

xTa

b10

0m

g5

Sulp

hon

amid

esan

dot

her

Bac

t.

Cip

la0.

00

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

252

Tabl

eB

.4Pr

ice

chan

ges

tod

rugs

for

mal

aria

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Ch

loro

qu

ine

yes

Emq

uin

Tab

250

mg

10A

nti

mal

aria

lsM

erck

7.29

−16.

14C

hlo

roq

uin

eye

sEm

qu

inTa

b25

0m

g10

00A

nti

mal

aria

lsM

erck

0.00

Ch

loro

qu

ine

yes

Emq

uin

D.S

.50

0m

g20

×5

An

tim

alar

ials

Mer

ck−3

.07

Ch

loro

qu

ine

yes

Emq

uin

Susp

160

mg/

10m

l60

ml

An

tim

alar

ials

Mer

ck1.

97

Ch

loro

qu

ine

yes

Emq

uin

Inj

64.5

mg/

ml

15×

30m

lA

nti

mal

aria

lsM

erck

9.19

Ch

loro

qu

ine

yes

Mel

ubr

inTa

b25

0m

g10

An

tim

alar

ials

Ran

baxy

−2.5

80.

00C

hlo

roq

uin

eye

sN

ivaq

uin

eTa

b25

0m

g10

An

tim

alar

ials

Nic

hol

asPi

ram

al−1

6.13

Ch

loro

qu

ine

yes

Niv

aqu

ine

Susp

80.6

5m

g/5

ml

60m

lA

nti

mal

aria

lsN

ich

olas

Pira

mal

−7.2

9

Ch

loro

qu

ine

yes

yes

Niv

aqu

ine

Inj

40m

g/m

l2

ml

amp

An

tim

alar

ials

Nic

hol

asPi

ram

al20

.33

Ch

loro

qu

ine

yes

yes

Niv

aqu

ine

Inj

40m

g/m

l5

mla

mp

An

tim

alar

ials

Nic

hol

asPi

ram

al5.

88

Ch

loro

qu

ine

yes

yes

Niv

aqu

ine

Inj

40m

g/m

l30

ml

An

tim

alar

ials

Nic

hol

asPi

ram

al5.

41

Mefl

oqu

ine

Mefl

iam

Tab

250

mg

6A

nti

mal

aria

lsC

ipla

0.00

Mefl

oqu

ine

Faci

tal

Tab

250

mg

6A

nti

mal

aria

lsC

adil

a0.

00Q

uin

ine

sulp

hat

eye

sK

un

enTa

b30

0m

g10

An

tim

alar

ials

Mer

rin

d0.

00Q

uin

ine

sulp

hat

eK

un

enTa

b60

0m

g10

An

tim

alar

ials

Mer

rin

d0.

00

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

253

Tabl

eB

.5Pr

ice

chan

ges

tod

rugs

for

HIV

/AID

S

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Zid

ovu

din

eye

sZi

dov

irC

ap10

0m

g10

An

tire

torv

iral

sC

ipla

−7.6

70.

00Zi

dov

ud

ine

yes

Zid

ovir

Cap

100

mg

100

An

tire

torv

iral

sC

ipla

0.00

Zid

ovu

din

eye

sZi

dov

irC

ap30

0m

g10

An

tire

torv

iral

sC

ipla

0.00

Zid

ovu

din

eye

sZi

dov

irC

ap30

0m

g60

An

tire

torv

iral

sC

ipla

0.00

Zid

ovu

din

eZi

dov

irSy

rup

50m

g/m

l10

0m

lA

nti

reto

rvir

als

Cip

la−3

3.33

Zid

ovu

din

eZi

dom

axC

ap10

0m

g10

An

tire

torv

iral

sA

lkem

0.00

Zid

ovu

din

eye

sZi

dom

axTa

b30

0m

g10

An

tire

torv

iral

sA

lkem

0.00

Zid

ovu

din

eZy

dow

inC

ap10

0m

g10

An

tire

torv

iral

sZy

du

sV

acci

care

0.00

Zid

ovu

din

eye

sZy

dow

inTa

b30

0m

g10

An

tire

torv

iral

sZy

du

sV

acci

care

0.00

Stav

ud

ine

yes

Stav

irC

ap30

mg

10A

nti

reto

rvir

als

Cip

la0.

00St

avu

din

eye

sSt

avir

Tab

40m

g10

An

tire

torv

iral

sC

ipla

0.00

Lam

ivu

din

e+

Zid

ovu

din

eye

sC

ombi

vir

Tab

150

mg

+ 300

mg

10A

nti

reto

rvir

als

GSK

0.00

Lam

ivu

din

e+

Zid

ovu

din

eye

sD

uov

irTa

b15

0m

g+ 30

0m

g

60A

nti

reto

rvir

als

Cip

la0.

00

Lam

ivu

din

e+

Zid

ovu

din

eye

sLa

mu

zid

Tab

150

mg

+ 300

mg

10A

nti

reto

rvir

als

Zyd

us

Vac

cica

re0.

00

Lam

ivu

din

e+

Zid

ovu

din

eye

sZi

dol

amTa

b15

0m

g+ 30

0m

g

10A

nti

reto

rvir

als

Gen

ix−2

3.64

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

254

Tabl

eB

.6Pr

ice

chan

ges

tod

rugs

for

Tube

rcu

losi

s

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Rif

amp

icin

+Is

onia

zid

yes

yes

Rim

paz

idTa

b45

0m

g+

300

mg

10A

nti

tube

rcu

losi

sC

adil

aH

ealt

h12

.39

0.00

Rif

amp

icin

+Is

onia

zid

yes

yes

Rim

acta

zid

450/

300

Tab

450

mg

+30

0m

g20

×4

An

titu

berc

ulo

sis

Nov

arti

s−1

2.17

Rif

amp

icin

+Is

onia

zid

yes

yes

Rim

acta

zid

Dis

ped

100

mg

+50

mg

10A

nti

tube

rcu

losi

sN

ovar

tis

−12.

19

Rif

amp

icin

+Is

onia

zid

yes

yes

Rim

acta

zid

Plu

sTa

b60

0m

g+

300

mg

25×

4A

nti

tube

rcu

losi

sN

ovar

tis

−12.

13

Rif

amp

icin

yes

yes

Rim

acta

ne

Cap

300

mg

4A

nti

tube

rcu

losi

sN

ovar

tis

2.90

0.00

Rif

amp

icin

yes

yes

Rim

acta

ne

Tab

450

mg

20×

4A

nti

tube

rcu

losi

sN

ovar

tis

−11.

07Et

ham

buto

l+

INH

yes

Myc

onex

800

Tab

800

mg

+30

0m

g10

An

titu

berc

ulo

sis

LeSa

nte

0.00

4.17

Eth

ambu

tol+

INH

yes

Inab

uto

lFo

rte

Tab

800

mg

+30

0m

g10

An

titu

berc

ulo

sis

Th

emis

Ch

emic

als

9.96

0.00

Eth

ambu

tol+

INH

yes

Com

bun

exTa

b80

0m

g+

300

mg

10A

nti

tube

rcu

losi

sLu

pin

13.4

50.

00

Pyra

zin

amid

eye

sP-

Zid

eTa

b50

0m

g10

An

titu

berc

ulo

sis

LeSa

nte

0.00

0.00

Pyra

zin

amid

eye

sP-

Zid

eTa

b75

0m

g11

An

titu

berc

ulo

sis

LeSa

nte

0.00

0.00

Pyra

zin

amid

eye

sP-

Zid

eTa

b10

00m

g12

An

titu

berc

ulo

sis

LeSa

nte

0.00

0.00

Pyra

zin

amid

eye

sPZ

A-C

iba

Tab

500

mg

10A

nti

tube

rcu

losi

sN

ovar

tis

7.56

0.00

Pyra

zin

amid

eye

sPZ

A-C

iba

Tab

750

mg

10A

nti

tube

rcu

losi

sN

ovar

tis

0.00

Pyra

zin

amid

eye

sPZ

A-C

iba

Tab

1000

mg

10A

nti

tube

rcu

losi

sN

ovar

tis

0.00

Pyra

zin

amid

ePZ

A-C

iba

Susp

5%10

0m

lA

nti

tube

rcu

losi

sN

ovar

tis

0.00

Stre

pto

myc

inye

sye

sA

mbi

stry

n-S

Inj

0.75

gmvi

alA

nti

tube

rcu

losi

sN

ich

olas

Pira

mal

8.96

−7.3

1St

rep

tom

ycin

yes

yes

Am

bist

ryn

-SIn

j1.

00gm

vial

An

titu

berc

ulo

sis

Nic

hol

asPi

ram

al−8

.15

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

255

Tabl

eB

.7Pr

ice

chan

ges

tod

rugs

for

alim

enta

ry,m

usc

ulo

-ske

leta

ld

isor

der

s,h

orm

ones

,an

dge

nit

o-u

rin

ary

syst

em

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Nal

idix

icA

cid

yes

yes

Gra

mon

egTa

b50

0m

g8

An

tid

iarr

hoe

als

Rex

tar

−0.4

10.

00N

alid

ixic

Aci

dye

sG

ram

oneg

Syru

p30

0m

g/5

ml

30m

lA

nti

dia

rrh

oeal

sR

exta

r0.

00

Nal

idix

icA

cid

+M

etro

nid

a-zo

le

yes

Gra

mon

eg–

MSy

rup

150

mg

+10

0m

g/5

ml

30m

lA

nti

dia

rrh

oeal

sR

anba

xy0.

00

Nal

idix

icA

cid

+M

etro

nid

a-zo

le

yes

yes

Gra

mon

eg–

MTa

b30

0m

g+

200

mg

8A

nti

dia

rrh

oeal

sR

anba

xy0.

00

Nor

flox

acin

+Ti

nid

azol

eye

sye

sG

ram

oneg

–T

NTa

b40

0m

g+

600

mg

10A

nti

dia

rrh

oeal

sR

anba

xy0.

00

Nal

idix

icA

cid

yes

Neg

adix

Tab

Kid

125

mg

10U

rin

ary

anti

-in

fect

ives

CFL

Phar

ma

−0.3

80.

00

Nal

idix

icA

cid

+M

etro

nid

a-zo

le

yes

yes

Neg

adix

–M

Tab

300

mg

+20

0m

g6

Uri

nar

yan

ti-i

nfe

ctiv

esC

FLPh

arm

a0.

00

Nal

idix

icA

cid

+M

etro

nid

a-zo

le

yes

Neg

adix

–M

Susp

150

mg

+10

0m

g60

ml

Uri

nar

yan

ti-i

nfe

ctiv

esC

FLPh

arm

a0.

00

Oxy

toci

nye

sPi

toci

nIn

j10

i.u

.1

amp

Dru

gsac

tin

gon

ute

rus

Pfize

r0.

7720

.51

Gli

ben

clam

ide

yes

Eugl

uco

nTa

b5

mg

10H

yper

and

hyp

ogly

caem

ics

Nic

hol

asPi

ram

al8.

3533

.33

Gli

ben

clam

ide

yes

Dao

nil

Tab

5m

g10

Hyp

eran

dh

ypog

lyca

emic

sSa

nofi

-Ave

nti

s6.

810.

00

256

Tabl

eB

.7(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Fru

sem

ide

yes

yes

Fru

sen

exTa

b40

mg

10D

iure

tics

and

An

tid

iure

tics

Gen

o−1

.03

0.00

Fru

sem

ide

yes

Fru

sen

exTa

b10

0m

g10

Diu

reti

csan

dA

nti

diu

reti

csG

eno

0.00

Fru

sem

ide

yes

yes

Lasi

xTa

b40

mg

10D

iure

tics

and

An

tid

iure

tics

San

ofi-A

ven

tis

−1.6

6

Fru

sem

ide

yes

Lasi

xTa

bH

igh

dos

e10

Diu

reti

csan

dA

nti

diu

reti

csSa

nofi

-Ave

nti

s0.

00

Fru

sem

ide

yes

yes

Lasi

xIn

j10

mg/

2m

l2

ml

Am

pD

iure

tics

and

An

tid

iure

tics

San

ofi-A

ven

tis

1.41

Fru

sem

ide

yes

yes

Lasi

xIn

jH

igh

dos

e10

mg

25m

lD

iure

tics

and

An

tid

iure

tics

San

ofi-A

ven

tis

0.00

Fru

sem

ide

+A

mil

orid

eye

sFr

um

ilTa

b40

mg

+5

mg

10D

iure

tics

and

An

tid

iure

tics

Gen

o8.

240.

00

Spir

onol

acto

ne

yes

yes

Ald

acto

ne

Tab

25m

g10

Diu

reti

csan

dA

nti

diu

reti

csR

PG4.

34−6

.04

Spir

onol

acto

ne

yes

Ald

acto

ne

Tab

100

mg

10D

iure

tics

and

An

tid

iure

tics

RPG

−8.1

7

Spir

onol

acto

ne

+H

ydro

flu

me-

thia

zid

e

yes

yes

Ald

acti

de

Tab

25m

g+

25m

g10

Diu

reti

csan

dA

nti

diu

reti

csR

PG0.

00

Ibu

pro

fen

yes

yes

Bru

fen

Tab

200

mg

10N

on-S

tero

idan

ti-i

nlm

.D

rugs

Abb

ott

4.66

0.00

Ibu

pro

fen

yes

yes

Bru

fen

Tab

400

mg

10N

on-S

tero

idan

ti-i

nlm

.D

rugs

Abb

ott

0.00

257

Ibu

pro

fen

yes

Bru

fen

Tab

600

mg

10N

on-S

tero

idan

ti-i

nlm

.Dru

gsA

bbot

t0.

00

Ibu

pro

fen

+Pa

race

tam

olye

sye

sC

ombi

flam

Tab

400

mg

+32

5m

g10

Non

-Ste

roid

anti

-in

lm.D

rugs

San

ofi-A

ven

tis

7.16

−1.6

7

Ibu

pro

fen

+Pa

race

tam

olye

sC

ombi

flam

Susp

100

mg

+16

2.5

mg/

5m

l60

ml

Non

-Ste

roid

anti

-in

lm.D

rugs

San

ofi-A

ven

tis

−1.6

2

Insu

lin

NPH

yes

yes

Act

rap

idIn

j40

i.u

.10

ml

Hyp

eran

dh

ypog

lyca

emic

sA

bbot

t3.

990.

00

Insu

lin

NPH

yes

yes

Act

rap

idM

CIn

j40

i.u

.10

ml

Hyp

eran

dh

ypog

lyca

emic

sA

bbot

t0.

00

Insu

lin

NPH

yes

yes

Len

tard

Inj

40i.

u./

ml

10m

lT

hro

idan

dan

tith

roid

dru

gsA

bbot

t1.

240.

00

Insu

lin

NPH

yes

yes

Ilet

in–

LIn

j40

i.u

./m

l10

ml

Th

roid

and

anti

thro

idd

rugs

Eli

Lill

y0.

00

Insu

lin

NPH

yes

yes

Ilet

in–

NPH

Inj

40i.

u./

ml

10m

lT

hro

idan

dan

tith

roid

dru

gsEl

iLi

lly

0.00

Insu

lin

NPH

yes

yes

Ilet

in–

RIn

j40

i.u

./m

l10

ml

Th

roid

and

anti

thro

idd

rugs

Eli

Lill

y0.

00

Pred

nis

olon

eye

sye

sW

ysol

one

Tab

5m

g10

Cor

tico

ster

oid

san

dre

late

dd

rugs

Wye

th−5

.10

0.00

Pred

nis

olon

eye

sye

sW

ysol

one

Tab

10m

g10

Cor

tico

ster

oid

san

dre

late

dd

rugs

Wye

th0.

00

Pred

nis

olon

eye

sW

ysol

one

Tab

20m

g10

Cor

tico

ster

oid

san

dre

late

dd

rugs

Wye

th0.

00

Pred

nis

olon

eye

sW

ysol

one

Tab

30m

g10

Cor

tico

ster

oid

san

dre

late

dd

rugs

Wye

th0.

00

Pred

nis

olon

eye

sW

ysol

one

Tab

40m

g10

Cor

tico

ster

oid

san

dre

late

dd

rugs

Wye

th0.

00

258

Tabl

eB

.7(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Mag

nes

ium

+ye

sPe

pti

cain

eLi

qu

idC

ombi

nat

ion

120

ml

Gas

tro-

inte

stin

alse

dat

ives

and

Ulc

erd

rugs

Pfize

r3.

440.

00

Mag

nes

ium

+ye

sSo

laci

dTa

bC

ombi

nat

ion

10G

astr

o-in

test

inal

sed

ativ

esan

dU

lcer

dru

gs

Dey

’sPh

arm

a10

.60

25.0

0

Mag

nes

ium

+ye

sSo

laci

dSy

rup

Com

bin

atio

n17

0m

lG

astr

o-in

test

inal

sed

ativ

esan

dU

lcer

dru

gs

Dey

’sPh

arm

a19

.40

Mag

nes

ium

+ye

sSo

laci

dSy

rup

Com

bin

atio

n34

0m

lG

astr

o-in

test

inal

sed

ativ

esan

dU

lcer

dru

gs

Dey

’sPh

arm

a18

.42

Mag

nes

ium

+ye

sSo

laci

d–

OSu

spC

ombi

nat

ion

170

ml

Gas

tro-

inte

stin

alse

dat

ives

and

Ulc

erd

rugs

Dey

’sPh

arm

a14

.28

Not

e:T

he

+sy

mbo

lat

the

end

ofa

dru

gn

ame

den

otes

form

ula

tion

sm

ade

from

mor

eth

anth

ree

dru

gs.

Wh

ile

all

the

dru

gsw

ere

con

sid

ered

for

the

anal

ysis

,it

was

con

sid

ered

app

rop

riat

eto

lim

itth

eli

stin

gto

thre

ed

rugs

for

this

stu

dy.

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

259

Tabl

eB

.8Pr

ice

chan

ges

tod

rugs

for

nu

trit

ion

and

resp

irat

ory

syst

em

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Vit

amin

Aye

sye

sR

ovig

onTa

bV

itam

inA

10,0

00i.

u+

Vit

amin

E25

mg

10V

itam

ins

Nic

hol

asPi

ram

al0.

440.

00

Salm

eter

olSe

robi

dIn

hal

er25

mcg

/m

eter

edd

ose

200

md

iB

ron

chos

pas

mC

ipla

3.40

0.00

Salm

eter

olSe

robi

dR

otah

aler

30B

ron

chos

pas

mC

ipla

0.00

Salm

eter

olSe

robi

dR

otac

ap50

mcg

30B

ron

chos

pas

mC

ipla

0.00

Salm

eter

olSa

lmet

erIn

hal

er25

mcg

/m

eter

edd

ose

Bro

nch

osp

asm

DR

L−0

.67

0.00

Eph

edri

ne

+T

heo

ph

ylli

ne

+p

hen

obar

bito

ne

yes

yes

Asm

apax

Dep

otTa

b50

mg

+65

mg

+30

mg

10B

ron

chos

pas

mN

ich

olas

Pira

mal

−0.3

4−1

.63

Eph

edri

ne

+T

heo

ph

ylli

ne

+p

hen

obar

bito

ne

yes

yes

Ale

rgin

Tab

20m

g+

100

mg

+15

mg

10B

ron

chos

pas

mC

ipla

7.36

0.00

Iron

+(S

alts

/com

ple

x)ye

sA

nem

idox

Cap

Com

bin

atio

n3

×10

An

aem

ia;

Neu

trop

enia

Mer

ck14

.18

−1.3

2

Iron

+(S

alts

/com

ple

x)Im

fero

nLi

qu

idC

ombi

nat

ion

200

ml

An

aem

ia;

Neu

trop

enia

Shre

ya4.

367.

35

Iron

+(S

alts

/com

ple

x)Im

fero

nC

apC

ombi

nat

ion

15A

nae

mia

;N

eutr

open

iaSh

reya

64.4

7

260

Tabl

eB

.8(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Iron

dex

tran

+V

itam

inB

-12

+Fo

lic

acid

yes

Imfe

ron

Inj

50m

gof

elem

enta

lir

on+

12,5

00m

cg+

2.5

mg/

ml

2m

lA

nae

mia

;N

eutr

open

iaSh

reya

−6.4

3

Iron

dex

tran

+V

itam

inB

-12

+Fo

lic

acid

yes

Imfe

ron

Inj

50m

gof

elem

enta

lir

on+

12,5

00m

cg+

2.5

mg/

ml

10m

lA

nae

mia

;N

eutr

open

iaSh

reya

−0.8

0

Iron

dex

tran

+V

itam

inB

-12

yes

Imfe

ron

B–

12In

j50

mg

ofel

emen

tal

iron

+50

0m

cg/m

l

2m

lA

nae

mia

;N

eutr

open

iaSh

reya

0.00

Iron

dex

tran

+V

itam

inB

-12

+Fo

lic

acid

yes

Imfe

ron

F–

12In

j50

mg

ofel

emen

tal

iron

+50

0m

cg+

2.5

mg/

ml

20×

2m

lA

nae

mia

;N

eutr

open

iaSh

reya

12.4

0

Bu

des

onid

ePu

lmic

ort

Inh

aler

100

mcg

100

dos

esB

ron

chos

pas

mre

laxa

nts

Ast

raZe

nec

a8.

9338

.51

Bu

des

onid

ePu

lmic

ort

Inh

aler

100

mcg

400

dos

esB

ron

chos

pas

mre

laxa

nts

Ast

raZe

nec

a0.

00

Salb

uta

mol

yes

yes

Salm

aplo

nTa

b2

mg

10B

ron

chos

pas

mre

laxa

nts

Kh

and

elw

al4.

06−6

8.00

261

Salb

uta

mol

yes

yes

Salm

aplo

nTa

b4

mg

10B

ron

chos

pas

mre

laxa

nts

Kh

and

elw

al−7

0.40

Salb

uta

mol

yes

yes

Salb

etol

Tab

2m

g10

Bro

nch

osp

asm

rela

xan

tsFD

C2.

570.

00

Salb

uta

mol

yes

yes

Salb

etol

Tab

4m

g10

Bro

nch

osp

asm

rela

xan

tsFD

C0.

00

Car

boh

ydra

te+

yes

Ferr

adol

Food

Pow

der

Com

bin

atio

n20

0gm

sTo

nic

s;ap

pet

ite

stim

ula

nts

Pfize

r−2

.06

0.00

Car

boh

ydra

te+

yes

Ferr

adol

Food

Pow

der

Com

bin

atio

n45

0gm

sTo

nic

s;ap

pet

ite

stim

ula

nts

Pfize

r0.

00

Am

ino

acid

+G

lyci

ne

+So

rbit

ol

Ast

ymin

–3

Infu

sion

81.2

mg

+10

mg

+50

mg/

ml

200

ml

Ton

ics;

app

etit

est

imu

lan

tsTa

blet

Ind

ia11

.75

Am

ino

acid

+G

lyci

ne

+So

rbit

ol

Ast

ymin

–3

Am

p81

.2m

g+

10m

g+

50m

g/m

l

20m

lTo

nic

s;ap

pet

ite

stim

ula

nts

Tabl

etIn

dia

8.31

L-is

oleu

cin

e+A

stym

in–

SNIn

fusi

onC

ombi

nat

ion

200

ml

Ton

ics;

app

etit

est

imu

lan

tsTa

blet

Ind

ia10

.27

L-is

oleu

cin

e+ye

sA

stym

inSy

rup

Com

bin

atio

n11

0m

lTo

nic

s;ap

pet

ite

stim

ula

nts

Tabl

etIn

dia

21.3

7

L-is

oleu

cin

e+ye

sA

stym

inSy

rup

Com

bin

atio

n20

0m

lTo

nic

s;ap

pet

ite

stim

ula

nts

Tabl

etIn

dia

22.9

9

Vit

amin

A+

yes

yes

Ast

ymin

Fort

eC

apC

ombi

nat

ion

10×

2To

nic

s;ap

pet

ite

stim

ula

nts

Tabl

etIn

dia

2.05

13.5

2

Vit

amin

C+

yes

Ast

ymin

–C

Dro

ps

Com

bin

atio

n15

ml

Ton

ics;

app

etit

est

imu

lan

tsTa

blet

Ind

ia19

.89

Mag

nes

ium

+A

stym

in-M

Fort

eC

apC

ombi

nat

ion

10To

nic

s;ap

pet

ite

stim

ula

nts

Tabl

etIn

dia

16.9

8

Dex

tros

e+Le

clyt

ePo

wd

erC

ombi

nat

ion

30gm

sM

iner

alan

dp

aren

tera

ln

utr

itio

nal

sup

pl.

Alb

ert

Dav

id0.

000.

00

Dex

tros

e+Le

clyt

e–

GIn

jC

ombi

nat

ion

500

ml

Plas

ma

exp

and

ers

Alb

ert

Dav

id−3

9.20

262

Tabl

eB

.8(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Dex

tros

e+Le

clyt

e–

MIn

jC

ombi

nat

ion

500

ml

Plas

ma

exp

and

ers

Alb

ert

Dav

id−3

9.20

Dex

tros

e+Le

clyt

e–

PIn

jC

ombi

nat

ion

500

ml

Plas

ma

exp

and

ers

Alb

ert

Dav

id−3

9.20

Dex

tros

e+Le

clyt

e–

RIn

jC

ombi

nat

ion

500

ml

Plas

ma

exp

and

ers

Alb

ert

Dav

id0.

00

Dex

tros

e+Le

clyt

e–

WPo

wd

erC

ombi

nat

ion

27.5

gms

Min

eral

and

par

ente

ral

nu

trit

ion

alsu

pp

l.

Alb

ert

Dav

id0.

00

Cal

ciu

mC

arbo

nat

e+

Vit

amin

D3

Oss

ivit

eTa

b0.

625

g+10

0i.

u.

10M

iner

alan

dp

aren

tera

ln

utr

itio

nal

sup

pl.

Wye

th5.

620.

00

Cal

ciu

mC

arbo

nat

e+

Vit

amin

D3

Oss

ivit

eTa

b1.

25g+

200

i.u

.10

Min

eral

and

par

ente

ral

nu

trit

ion

alsu

pp

l.

Wye

th0.

00

Vit

amin

A+

yes

yes

Fili

bon

Cap

Com

bin

atio

n50

Min

eral

and

par

ente

ral

nu

trit

ion

alsu

pp

l.

Wye

th2.

900.

00

Dex

trom

eth

rop

han

+G

rili

nct

us

Syru

pC

ombi

nat

ion

100

ml

Exp

ecto

ran

ts,

Cou

ghSu

pp

r.,

Dec

onge

stan

ts

Fran

coIn

dia

n4.

6753

.66

Dex

trom

eth

rop

han

+G

rili

nct

us

Syru

pC

ombi

nat

ion

450

ml

Exp

ecto

ran

ts,

Cou

ghSu

pp

r.,

Dec

onge

stan

ts

Fran

coIn

dia

n25

.00

Terb

uta

lin

e+

Bro

mh

exci

ne

Gri

lin

ctu

sB

MSy

rup

2.5

mg

+8

mg/

5m

l10

0m

lEx

pec

tora

nts

,C

ough

Sup

pr.

,D

econ

gest

ants

Fran

coIn

dia

n25

.00

Terb

uta

lin

e+

Bro

mh

exci

ne

Gri

lin

ctu

sB

MPe

adsy

rup

1.5

mg

+4

mg/

5m

l30

ml

Exp

ecto

ran

ts,

Cou

ghSu

pp

r.,

Dec

onge

stan

ts

Fran

coIn

dia

n16

.86

263

Terb

uta

lin

e+

Bro

mh

exci

ne

yes

Gri

lin

ctu

sB

MTa

b2.

5m

g+

8m

g/5

ml

10Ex

pec

tora

nts

,Cou

ghSu

pp

r.,D

econ

gest

ants

Fran

coIn

dia

n43

.40

Terb

uta

lin

e+B

ro-Z

edex

Syru

pC

ombi

nat

ion

100

ml

Exp

ecto

ran

ts,C

ough

Sup

pr.

,Dec

onge

stan

tsW

ockh

ard

t5.

690.

00

Terb

uta

lin

e+B

ro-Z

edex

Liq

uic

apC

ombi

nat

ion

6Ex

pec

tora

nts

,Cou

ghSu

pp

r.,D

econ

gest

ants

Woc

khar

dt

0.00

Ch

lorp

hen

iram

ine

+A

mm

oniu

mch

lori

de

+So

diu

mci

trat

e

Piri

ton

Exp

ecto

ran

tLi

qu

id2.

5m

g+

125

mg

+55

mg/

5m

l

120

ml

Exp

ecto

ran

ts,c

ough

sup

pre

ssan

ts,m

uco

lyti

csan

dd

econ

gest

ants

GSK

5.42

0.00

Ch

lorp

hen

iram

ine

+A

mm

oniu

mch

lori

de

+So

diu

mci

trat

e

Piri

ton

Exp

ecto

ran

tLi

qu

id2.

5m

g+

125

mg

+55

mg/

5m

l

460

ml

Exp

ecto

ran

ts,c

ough

sup

pre

ssan

ts,m

uco

lyti

csan

dd

econ

gest

ants

GSK

3.00

Ch

lorp

hen

iram

ine

+C

odei

ne

Cor

exSy

rup

4m

g+

10m

g/5

ml

50m

lEx

pec

tora

nts

,cou

ghsu

pp

ress

ants

,mu

coly

tics

and

dec

onge

stan

ts

Pfize

r−0

.24

24.2

7

Ch

lorp

hen

iram

ine

+C

odei

ne

Cor

exSy

rup

4m

g+

10m

g/5

ml

100

ml

Exp

ecto

ran

ts,c

ough

sup

pre

ssan

ts,m

uco

lyti

csan

dd

econ

gest

ants

Pfize

r24

.00

Dex

trom

eth

orp

han

+C

hlo

rph

enir

amin

e+

Men

thol

Cor

ex–

DX

Syru

p10

mg

+4

mg

+0.

1m

g/5

ml

50m

lEx

pec

tora

nts

,cou

ghsu

pp

ress

ants

,mu

coly

tics

and

dec

onge

stan

ts

Pfize

r30

.23

Dex

trom

eth

orp

han

+C

hlo

rph

enir

amin

e+

Men

thol

Cor

ex–

DX

Syru

p10

mg

+4

mg

+0.

1m

g/5

ml

100

ml

Exp

ecto

ran

ts,c

ough

sup

pre

ssan

ts,m

uco

lyti

csan

dd

econ

gest

ants

Pfize

r30

.50

Not

e:T

he

+sy

mbo

lat

the

end

ofa

dru

gn

ame

den

otes

form

ula

tion

sm

ade

from

mor

eth

anth

ree

dru

gs.

Wh

ile

all

the

dru

gsw

ere

con

sid

ered

for

the

anal

ysis

,it

was

con

sid

ered

app

rop

riat

eto

lim

itth

eli

stin

gto

thre

ed

rugs

for

this

stu

dy.

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

264

Tabl

eB

.9Pr

ice

chan

ges

tod

rugs

for

ENT,

skin

,an

dsu

rgic

alan

aest

het

ics

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Lign

ocai

ne+

yes

Xyl

ocai

ne

cA

dre

nal

ine

Inj

Com

bin

atio

n30

ml

An

aest

het

ics

Ast

raZe

nec

a6.

4443

.95

Lign

ocai

ne

+M

eth

ylp

arab

enye

sX

yloc

ain

ec

Ad

ren

alin

eTo

pic

al4%

42.7

mg/

ml

+1

mg/

ml

30m

lA

nae

sth

etic

sA

stra

Zen

eca

51.4

2

Lign

ocai

ne

+M

eth

ylp

arab

en+

Sod

ium

chlo

rid

e

yes

Xyl

ocai

ne

1%In

j10

.7m

g+

1m

g+

6m

g/m

l

30m

lA

nae

sth

etic

sA

stra

Zen

eca

47.5

1

Lign

ocai

ne

+M

eth

ylp

arab

enye

sX

yloc

ain

e1%

Inj

21.3

mg

+1

mg

+6

mg/

ml

30m

lA

nae

sth

etic

sA

stra

Zen

eca

35.4

0

Lign

ocai

ne

+M

eth

ylp

arab

en+

Prop

ylp

arab

en

Xly

ocai

ne

Jell

y2%

Gel

21.3

mg

+0.

61m

g+

0.27

mg/

ml

30gm

sA

nae

sth

etic

sA

stra

Zen

eca

35.9

0

Lign

ocai

ne

+Pr

opyl

ene

glyc

olye

sX

yloc

ain

eO

int

5%O

intm

ent

5%w

/w+

25%

w/w

20gm

sA

nae

sth

etic

sA

stra

Zen

eca

43.9

5

Lign

ocai

ne

+Et

han

olX

yloc

ain

eSp

ray

Spra

y10

0m

g+

28.2

9%v/

vp

erm

l

500

md

An

aest

het

ics

Ast

raZe

nec

a0.

00

Lign

ocai

ne

+M

eth

ylp

arab

enX

yloc

ain

eSp

ray

100

mg

+28

.29%

v/v

per

ml

800

md

An

aest

het

ics

Ast

raZe

nec

a0.

00

Lign

ocai

ne

+M

eth

ylp

arab

en+

Prop

ylp

arab

en

yes

Vis

cou

s2%

Vis

cou

s21

.3m

g+

0.61

mg

+0.

27m

g/m

l

100

ml

An

aest

het

ics

Ast

raZe

nec

a50

.99

Lign

ocai

ne

+So

diu

mch

lori

de

yes

Xyl

ocar

dV

ial

21.3

mg

+6

mg/

ml

50m

lV

entr

icu

lar

arrh

yth

mia

sA

stra

Zen

eca

50.9

6

265

Lign

ocai

ne

+D

extr

ose

yes

Xyl

ocai

ne

Hea

vy5%

Inj

53.5

mg

+75

mg

25×

2m

lSp

inal

anae

sth

esia

Ast

raZe

nec

a0.

00

Lign

ocai

ne

+G

luco

seye

sG

esic

ain

Hea

vy5%

Inj

5%+

7.5%

25×

2m

lSp

inal

anae

sth

esia

Nic

hol

asPi

ram

al5.

51

Lign

ocai

ne

yes

Ges

icai

nc

Ad

ren

alin

e2%

Inj

2%30

ml

An

aest

het

ics

Nic

hol

asPi

ram

al9.

990.

00

Lign

ocai

ne

yes

Ges

icai

nIn

j2%

30m

lA

nae

sth

etic

sN

ich

olas

Pira

mal

0.00

Lign

ocai

n+

Car

boxy

-m

eth

ylce

llu

lose

Ges

icai

nJe

lly

2%G

el2%

+3.

5%30

ml

An

aest

het

ics

Nic

hol

asPi

ram

al0.

00

Ligo

cain

eye

sG

esic

ain

Oin

t5%

Oin

tmen

t5%

10gm

An

aest

het

ics

Nic

hol

asPi

ram

al5.

49

Ligo

cain

eye

sG

esic

ain

Top

ical

4%SO

LN

Soln

4%30

ml

An

aest

het

ics

Nic

hol

asPi

ram

al5.

49

Ket

amin

eye

sK

etm

inIn

j10

mg/

ml

10m

lA

nae

sth

etic

sT

hem

isM

edic

are

−3.5

80.

00

Ket

amin

eye

sK

etm

inIn

j50

mg/

ml

2m

lA

nae

sth

etic

sT

hem

isM

edic

are

0.00

Ket

amin

eye

sK

etal

arIn

j10

mg

20m

lA

nae

sth

etic

sPfi

zer

0.00

0.00

Ket

amin

eye

sK

etal

arIn

j50

mg

2m

lA

nae

sth

etic

sPfi

zer

0.00

Ket

amin

eye

sK

etal

arIn

j50

mg

10m

lA

nae

sth

etic

sPfi

zer

0.00

Lign

ocai

ne+

yes

Ote

k-A

C+

Dro

ps

Com

bin

atio

n5

ml

An

ti-i

nfe

ctiv

ep

rep

.FD

C7.

8828

.42

Ch

lora

mp

hen

icol

Ch

loro

myc

etin

Ap

lica

ps

Ap

lica

ps

(eye

)25

0mg

50A

nti

-in

fect

ive

pre

pPfi

zer

27.4

8

Ch

lora

mp

hen

icol

+B

enzo

cain

eC

hlo

rom

ycet

inD

rop

s(e

ye)

5%w

/v+

1%w

/v5

ml

An

ti-i

nfe

ctiv

ep

rep

Pfize

r0.

00

Ch

lora

mp

hen

icol

+B

enzo

cain

e+

Prop

ylen

egl

ycol

Ch

loro

myc

etin

Dro

ps

(ear

)5%

w/v

+1%

w/v

+q

.s

5m

lA

ura

lPr

epar

atio

ns

Pfize

r24

.49

Gen

tam

ycin

+B

enza

lkon

ium

yes

yes

Gen

ticy

nEy

e/Ea

rD

rop

sG

enta

myc

in0.

3%5

ml

Au

ral

Prep

arat

ion

sN

ich

olas

Pira

mal

0.27

266

Tabl

eB

.9(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Gen

tam

ycin

+B

enza

lkon

ium

yes

yes

Gen

ticy

nE/

ED

rop

s0.

3%+

0.04

%5

ml

An

ti-i

nfe

ctiv

ep

rep

All

erga

n3.

260.

00

Gen

tam

ycin

+ye

sye

sG

enti

cyn

BEy

e/Ea

rD

rop

sC

ombi

nat

ion

5m

lA

nti

-in

flam

ator

y/A

nti

-all

ergi

cN

ich

olas

Pira

mal

0.00

Gen

tam

ycin

+ye

sye

sG

enti

cyn

HC

Dro

ps

Com

bin

atio

n5

ml

An

ti-i

nfl

amat

ory/

An

ti-a

ller

gic

Nic

hol

asPi

ram

al0.

00

Flu

tica

son

eZo

flu

tC

ream

0.05

%5

gmTo

pic

alst

eroi

dPr

epC

ipla

1.22

0.00

Flu

tica

son

eZo

flu

tC

ream

0.05

%10

gmTo

pic

alst

eroi

dPr

epC

ipla

0.00

Flu

tica

son

eZo

flu

tLo

tion

0.05

%10

ml

Top

ical

ster

oid

Prep

Cip

la0.

00Fl

uti

caso

ne

Zofl

ut

Oin

tmen

t0.

05%

10gm

Top

ical

ster

oid

Prep

Cip

la0.

00N

itro

fura

zon

eFu

raci

n-S

Cre

am0.

02%

20gm

sTo

pic

alst

eroi

dPr

epG

SK0.

00−2

8.87

Nit

rofu

razo

ne

Fura

cin

-SC

ream

0.02

%50

0gm

sTo

pic

alst

eroi

dPr

epG

SK−4

.28

Cro

tam

iton

+H

ydro

cort

ison

eC

roto

rax-

HC

Cre

am10

%+

0.25

%10

gms

Top

ical

ster

oid

Prep

Nic

hol

asPi

ram

al0.

180.

00

Cro

tam

iton

Cro

tora

xC

ream

10%

20gm

sTo

pic

alst

eroi

dPr

epN

ich

olas

Pira

mal

0.00

Cro

tam

iton

Cro

tora

xLo

tion

10%

60m

lTo

pic

alst

eroi

dPr

epN

ich

olas

Pira

mal

0.00

Hep

arin

+B

enzy

ln

icot

inat

eB

epar

ine

Cre

am50

.i.u

+3

mg/

g15

gmM

isc.

skin

pre

p.

Bio

logi

cal

E8.

450.

20

Sod

ium

dia

triz

oate

+M

eglu

min

ean

tim

onat

e

yes

Uro

grafi

n60

%/7

6%In

j16

00+

1040

0m

g20

ml

Dia

gnos

tic

Age

nts

Ger

man

Rem

edie

s18

.19

0.00

Sod

ium

dia

triz

oate

+M

eglu

min

ean

tim

onat

e

yes

Uro

grafi

n60

%/7

6%In

j20

00+

1320

0m

g20

ml

Dia

gnos

tic

Age

nts

Ger

man

Rem

edie

s0.

00

267

Bu

piv

acai

ne

yes

Mar

cain

eIn

j0.

50%

20m

lSu

rgic

alan

tiba

cter

ials

Nic

hol

asPi

ram

al2.

380.

00

Bu

piv

acai

ne

Mar

cain

eH

yper

bari

cIn

j1%

2m

lSu

rgic

alan

tiba

cter

ials

Nic

hol

asPi

ram

al0.

00

Bu

piv

acai

ne

+So

diu

mC

hlo

rid

e+

Met

hya

lp

arab

en

yes

Sen

sorc

ain

eIn

j0.

25%

2.64

+8

+1

mg/

ml

20m

lSu

rgic

alan

tiba

cter

ials

Ast

raZe

nec

a8.

4464

.98

Bu

piv

acai

ne

+So

diu

mC

hlo

rid

e+

Met

hyl

par

aben

yes

Sen

sorc

ain

eIn

j0.

25%

5.28

+8

+1

mg/

ml

20m

lSu

rgic

alan

tiba

cter

ials

Ast

raZe

nec

a0.

00

Bu

piv

acai

ne

+D

extr

ose

mon

ohyd

rate

yes

Sen

sorc

ain

eH

eavy

Inj

5+

80m

g/m

l5

×4

ml

Surg

ical

anti

bact

eria

lsA

stra

Zen

eca

0.00

Bu

piv

acai

ne

+ye

sSe

nso

rcai

ne

0.5%

wit

hA

dre

nal

ine

Inj

Com

bin

atio

n20

ml

Surg

ical

anti

bact

eria

lsA

stra

Zen

eca

0.00

Bec

lom

eth

ason

ed

ipro

pio

nat

eB

ecla

te–

200

Inh

aler

200

mg

200

md

Loca

lre

acta

nts

onth

en

ose

Cip

la1.

970.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

eye

sB

ecla

teIn

hal

erIn

hal

er50

mcg

200

dos

esLo

cal

reac

tan

tson

the

nos

e

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

eB

ecla

teIn

hal

erIn

hal

er10

0m

cg20

0d

oses

Loca

lre

acta

nts

onth

en

ose

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

eB

ecla

teR

otac

aps

Inh

aler

100

mcg

10Lo

cal

reac

tan

tson

the

nos

e

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

eB

ecla

teR

otac

aps

Inh

aler

200

mcg

30Lo

cal

reac

tan

tson

the

nos

e

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

e+

Ch

inof

orm

Bec

late

Rot

acap

sIn

hal

er40

0m

cg30

Loca

lre

acta

nts

onth

en

ose

Cip

la0.

00

268

Tabl

eB

.9(C

onti

nu

ed)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Bec

lom

eth

ason

ed

ipro

pio

nat

eB

ecla

te-C

Cre

am0.

025%

w/w

+3%

15gm

Top

ical

ster

oid

Prep

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

e+

Neo

myc

in

Bec

late

-NC

ream

0.02

5%+

0.5%

15gm

Top

ical

ster

oid

Prep

Cip

la0.

00

Bec

lom

eth

ason

ed

ipro

pio

nat

e+

Sali

cycl

icac

id

yes

Bec

late

-SO

intm

ent

0.1%

+3%

15gm

Top

ical

ster

oid

Prep

Cip

la0.

00

Atr

opin

e+

Pred

nis

olon

+C

hlo

robu

tan

ol

yes

Atr

isol

onD

rop

s1%

+0.

25%

+0.

5%

5m

lA

nti

-in

flam

mat

ory

and

anti

-all

ergi

cp

rep

.

Inta

s2.

310.

00

Not

e:T

he

+sy

mbo

lat

the

end

ofa

dru

gn

ame

den

otes

form

ula

tion

sm

ade

from

mor

eth

anth

ree

dru

gs.

Wh

ile

all

the

dru

gsw

ere

con

sid

ered

for

the

anal

ysis

,it

was

con

sid

ered

app

rop

riat

eto

lim

itth

eli

stin

gto

thre

ed

rugs

for

this

stu

dy.

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

269

Tabl

eB

.10

Pric

ech

ange

sto

dru

gsfo

rca

nce

ran

dot

her

rela

ted

trea

tmen

ts

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

All

opu

rin

olye

sZy

lori

cTa

b10

0m

g10

Gou

tG

SK4.

8013

.64

All

opu

rin

olZy

lori

cTa

b30

0m

g10

Gou

tG

SK0.

00B

leom

ycin

yes

Ble

ocin

Inj

15m

gV

ial

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

Kh

and

elw

al0.

85−9

.62

Ch

lora

mbu

cil

Leu

kera

nTa

b2

mg

25C

arci

no-

chem

oth

erap

euti

cD

rugs

GSK

8.87

0.00

Ch

lora

mbu

cil

Leu

kera

nTa

b5

mg

25C

arci

no-

chem

oth

erap

euti

cD

rugs

GSK

0.00

Cyc

lop

hos

ph

amid

eye

sEn

dox

an-A

sta

Tab

50m

g10

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

Ger

man

Rem

edie

s3.

640.

00

Cyc

lop

hos

ph

amid

eye

sEn

dox

an-A

sta

Inj

200

mg

Via

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Ger

man

Rem

edie

s0.

00

Cyc

lop

hos

ph

amid

eye

sEn

dox

an-A

sta

Inj

500

mg

Via

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Ger

man

Rem

edie

s0.

00

Cyc

lop

hos

ph

amid

eEn

dox

an-A

sta

Inj

1gm

Via

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Ger

man

Rem

edie

s0.

00

Dox

oru

bici

nye

sD

oxor

ubi

cin

-M

eiji

nIn

j10

mg

Via

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Kh

and

elw

al1.

100.

00

270

Tabl

eB

.10

(Con

tin

ued

)

Cat

ego

ryD

PC

ON

LE

MB

ran

dFo

rmSt

ren

gth

Qty

Th

erap

euti

cgr

ou

pC

om

pan

yP

rice

chan

ge%

Dru

gn

ame/

Yea

r19

9520

0319

94–2

004

2005

–200

8

Dox

oru

bici

nye

sD

oxor

ubi

cin

-M

eiji

nIn

j50

mg

Via

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Kh

and

elw

al0.

00

Etop

sid

e+

Ben

zyl

alco

hol

+Et

hyl

alco

hol

yes

Etos

idIn

j10

0m

g+

150

mg

+30

%/5

ml

5m

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Cip

la−0

.91

0.00

Etop

sid

e+

Ben

zyl

alco

hol

+Et

hyl

alco

hol

yes

Etos

idC

ap10

0m

g+

150

mg

+30

%/5

ml

4C

arci

no-

chem

oth

erap

euti

cD

rugs

Cip

la0.

00

Flu

orou

raci

lFl

ura

cil

Cap

250

mg

10C

arci

no-

chem

oth

erap

euti

cD

rugs

Bio

chem

0.71

0.00

Flu

orou

raci

lFl

ura

cil

Inj

500

mg

10m

l/2

×5

ml

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

Bio

chem

107.

40

Hep

arin

+B

enzy

ln

icot

inat

e

Th

rom

bop

hop

Oin

t50

00i.

u+

0.2/

100

g20

gmC

arci

no-

chem

oth

erap

euti

cD

rugs

Ger

man

Rem

edie

s0.

000.

00

Hep

arin

Th

rom

bop

hop

Gel

20,0

00i.

u/

100

g20

gmC

arci

no-

chem

oth

erap

euti

cD

rugs

Ger

man

Rem

edie

s0.

00

271

Met

hot

rexa

teye

sN

eotr

exat

eTa

b2.

5m

g10

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

GSK

0.00

6.20

Met

hot

rexa

teye

sB

iotr

exat

eTa

b2.

5m

g10

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

Bio

chem

1.04

−6.0

8

Met

hot

rexa

teye

sB

iotr

exat

eIn

j50

mg

2m

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Bio

chem

0.00

Tam

oxif

enye

sM

amof

enTa

b10

mg

10C

arci

no-

chem

oth

erap

euti

cD

rugs

Kh

and

elw

al0.

004.

62

Tam

oxif

enye

sN

olva

dex

Tab

10m

g50

Car

cin

o-ch

emot

her

apeu

tic

Dru

gs

Ast

raZe

nec

ca2.

840.

00

Vin

cris

tin

e+ye

sC

ytoc

rist

inIn

jC

ombi

nat

ion

1m

lC

arci

no-

chem

oth

erap

euti

cD

rugs

Cip

la1.

086.

67

Not

e:T

he

+sy

mbo

lat

the

end

ofa

dru

gn

ame

den

otes

form

ula

tion

sm

ade

from

mor

eth

anth

ree

dru

gs.

Wh

ile

all

the

dru

gsw

ere

con

sid

ered

for

the

anal

ysis

,it

was

con

sid

ered

app

rop

riat

eto

lim

itth

eli

stin

gto

thre

ed

rugs

for

this

stu

dy.

Sour

ce:

For

1994

–200

4M

IMS

Ind

ia,

asci

ted

inSa

kth

ivel

2006

,fo

r20

05–0

8,D

rug

Tod

ay,

vari

ous

issu

es,

CIM

SIn

dia

,20

07Ju

ly–O

ctob

er,

and

IDR

Phar

mac

yTr

ipp

leC

omp

end

ium

,200

8,N

ovem

ber

07–J

anu

ary

08.

Appendix C

Sensitivity test: Case 1

Payment schedule for the lowest income category remains unchanged. For theother categories, the co-payments are raised from Rs. 25 to Rs. 30 and from Rs. 50to Rs. 60. The Safety Net threshold is also raised from Rs. 1125 to Rs. 1350 andfrom Rs. 2000 to Rs. 2400.

272

273

Tabl

eC

.1En

titl

emen

tsof

Ind

iaH

ealt

hca

rds

ata

glan

ce

S.N

oIn

com

ep

.a.

Cat

ego

ryC

olo

ur

Co

-pay

men

tp

erp

resc

rip

tio

nSa

fety

Net

Th

resh

old

Co

-pay

men

t(p

ost

Safe

tyN

et)

per

pre

scri

pti

on

(Rs.

)(R

s.)

(Rs.

)(R

s.)

1N

one

S-C

ard

Bro

wn

Nil

N.A

.N

il2

<15

,000

B1-

Car

dR

edN

ilN

.AN

il3

15,0

01–4

0,00

0B

2-C

ard

Yell

ow10

500

Nil

415

,001

–40,

000

A1-

Car

dW

hit

e/Ye

llow

1050

0N

il5

40,0

01–1

00,0

00A

2-C

ard

Wh

ite/

Purp

le30

1350

106

40,0

01–1

00,0

00M

1-C

ard

Purp

le30

1350

107

>10

0,00

0A

3-C

ard

Wh

ite/

Gre

en60

2400

308

>10

0,00

0M

2-C

ard

Gre

en60

2400

30

Not

e:T

he

thre

shol

dw

ould

kick

inat

40p

resc

rip

tion

sfo

rB

2an

dA

1C

ateg

orie

s,at

45p

resc

rip

tion

sfo

rM

1an

dA

2ca

tego

ries

,an

dat

50p

resc

rip

tion

sfo

rM

2an

dA

3ca

tego

ries

.So

urce

:Au

thor

.

274

Tabl

eC

.2C

alcu

lati

ng

hea

lth

and

med

icin

eex

pen

dit

ure

(Rs.

)

Cat

ego

ryP

op

ula

tio

nH

ealt

h(m

on

thly

)M

edic

ine

(mo

nth

ly)

(Mil

lio

n.)

Per

cap

ita

(Rs.

)To

tal

Rs.

(Mil

lio

n.)

Per

cap

ita

(Rs.

)To

tal

Rs.

(Mil

lio

n.)

Ru

ral

798

4435

,112

28.1

622

,471

.68

Urb

an34

271

24,2

8239

.76

13,5

97.9

2To

tal

(In

dia

)11

4059

,394

36,0

69.6

Bas

edo

nth

eab

ove

Tab

leH

ealt

h(y

earl

y)M

edic

ine

(yea

rly)

Ru

ral

421,

344

269,

660.

2U

rban

291,

384

163,

175

Tota

l(I

nd

ia)

712,

728

432,

835.

2Pe

rp

erso

n62

5.2

379.

68Pe

rfa

mil

y31

2618

98.4

Sour

ce:A

uth

ores

tim

ates

base

don

GO

I(2

007c

,200

7f).

275

Tabl

eC

.3A

nn

ual

exp

end

itu

reon

med

icin

esu

nd

ercu

rren

tan

dp

rop

osed

mod

els

S.N

o.

Cat

ego

ryE

stim

ated

po

pu

lati

on

(mil

lio

n)

Est

imat

edn

o.

of

card

s(m

illi

on

)

Tota

ld

rug

exp

end

itu

re–

Ind

ia(R

s.m

illi

on

)

Tota

lo

ut-

of-

po

cket

co-p

aym

ents

(Rs.

mil

lio

n)

Go

vern

men

tco

ntr

ibu

tio

n(R

s.m

illi

on

)

Ave

rage

OO

Pm

ed.

exp

per

fam

ily

(Rs.

)

Ave

rage

ou

t-o

f-p

ock

etd

rug

exp

end

itu

rep

erfa

mil

y(R

s.)

(cu

rren

t)(p

rop

ose

d)

(pro

po

sed

)(p

rop

ose

d)

(cu

rren

t)1

23

45

67

=(5

−6)

89

1S-

Car

d40

40.0

015

,187

.20

15,1

87.2

018

98.4

2B

1-C

ard

350

86.5

013

2,88

80

132,

888

018

98.4

3B

2-C

ard

450

85.5

017

0,85

642

,750

128,

106

500

1898

.44

A1-

Car

d5

2.50

1,89

8.4

1,25

064

8.4

500

1898

.45

A2-

Car

d5

2.50

1,89

8.4

3,71

2.5

014

8518

98.4

6M

1-C

ard

190

38.0

072

,139

.256

,430

15,7

09.2

1485

1898

.47

A3-

Car

d5

2.50

1,89

8.4

6,60

00

2640

1898

.48

M2-

Car

d95

19.0

036

,069

.650

,160

026

4018

98.4

Tota

l11

4027

6.50

432,

835

160,

903

271,

933

582

1898

.410

0%37

.17

62.8

3

Not

e:A

t5

per

cen

t,17

.5m

illi

onel

der

lyp

opu

lati

onw

ould

beis

sued

wit

h8.

75m

illi

onB

1-C

ard

s.A

t5

mem

bers

per

fam

ily,

332.

5m

illi

onp

opu

lati

onw

ould

beis

sued

wit

h66

.5m

illi

onB

1-C

ard

s(A

ged

).A

t5

per

cen

tof

450

mil

lion

ofB

2-p

opu

lati

on,

22.5

mil

lion

eld

erly

pop

ula

tion

wou

ldbe

issu

edw

ith

11.2

5m

illi

onB

1-C

ard

s(A

ged

)T

hu

s,th

en

um

ber

ofca

rds

issu

edin

B1

cate

gory

wou

ldbe

hig

her

and

inB

2w

ould

belo

wer

than

stra

igh

tfo

rwar

dd

ivid

ing

the

tota

lp

opu

lati

onby

5in

thos

eca

tego

ries

.So

urce

:Au

thor

esti

mat

esba

sed

onG

OI

(200

7c,2

007f

).

276

Tabl

eC

.4Es

tim

ates

ofto

tal

out-

of-p

ocke

tm

edic

ine

exp

end

itu

re(R

s.m

illi

on)

and

pop

ula

tion

grou

ps

(mil

lion

)

Yea

rTo

tal

0–4

(fac

tor

1.2)

5–64

(fac

tor

1)65

+(f

acto

r4.

5)To

tal

OO

Pm

ed.

exp

Tota

lO

OP

med

exp

Incl

.5%

CA

GR

Po

pu

lati

on

Po

pu

lati

on

Med

.Ex

p.

Po

pu

lati

on

Med

.Ex

p.

Po

pu

lati

on

Med

.Ex

p.

12

34

56

78

9(4

+6

+8)

10

2006

1140

126.

557

,635

956.

536

3,16

457

.097

,388

518,

187

518,

187.

320

0711

6012

7.6

58,1

3797

3.8

369,

732

58.6

100,

122

527,

991

554,

390.

120

0811

8112

7.5

58,0

9199

3.2

377,

098

60.2

102,

855

538,

045

593,

194.

120

0912

0112

7.3

58,0

0010

11.2

383,

932

62.5

106,

785

548,

717

635,

208.

920

1012

2012

6.9

57,8

1810

28.5

390,

501

64.7

110,

544

558,

862

679,

300.

720

1112

3712

6.2

57,4

9910

44.0

396,

386

66.8

114,

132

568,

016

724,

948.

920

1212

5412

5.4

57,1

3410

59.6

402,

309

69.0

117,

891

577,

334

773,

682.

520

1312

7112

4.6

56,7

7010

75.3

408,

270

71.2

121,

649

586,

689

825,

530.

520

1412

8712

4.8

56,8

6110

88.8

413,

396

73.4

125,

408

595,

665

880,

068.

120

1513

0312

5.1

56,9

9811

02.3

418,

521

75.6

129,

167

604,

686

938,

066.

4

Sour

ce:A

uth

ores

tim

ates

base

don

Un

ited

Nat

ion

s(2

005a

);an

dG

OI

(200

7c,2

007f

).

277

Tabl

eC

.5Es

tim

ates

ofto

tal

out-

of-p

ocke

the

alth

exp

end

itu

re(R

s.m

illi

on)

and

pop

ula

tion

grou

ps

(mil

lion

)

Yea

rTo

tal

0–4

(fac

tor

1.2)

5–64

(fac

tor

1)65

+(f

acto

r4.

5)To

tal

OO

Ph

ealt

hex

p.

Tota

lO

OP

hea

lth

exp

.in

cl.

5%C

AG

RP

op

ula

tio

nP

op

ula

tio

nH

ealt

hex

p.

Po

pu

lati

on

Hea

lth

exp

.P

op

ula

tio

nH

ealt

hex

p.

12

34

56

78

9(4

+6

+8)

10

2006

1140

126.

594

,905

956.

559

8,00

457

160,

364

853,

273

853,

273

2007

1160

127.

695

,731

973.

860

8,82

058

.616

4,86

586

9,41

691

2,88

620

0811

8112

7.5

95,6

5699

3.2

620,

949

60.2

169,

367

885,

971

976,

783

2009

1201

127.

395

,506

1011

.263

2,20

262

.517

5,83

890

3,54

51,

045,

967

2010

1220

126.

995

,205

1028

.564

3,01

864

.718

2,02

792

0,25

11,

118,

570

2011

1237

126.

294

,680

1,04

465

2,70

966

.818

7,93

593

5,32

41,

193,

737

2012

1254

125.

494

,080

1059

.666

2,46

269

194,

125

950,

667

1,27

3,98

420

1312

7112

4.6

93,4

8010

75.3

672,

278

71.2

200,

314

966,

072

1,35

9,36

020

1412

8712

4.8

93,6

3010

88.8

680,

718

73.4

206,

504

980,

851

1,44

9,16

420

1513

0312

5.1

93,8

5511

02.3

689,

158

75.6

212,

693

995,

706

1,54

4,66

7

Sour

ce:A

uth

ores

tim

ates

base

don

Un

ited

Nat

ion

s(2

005a

);an

dG

OI

(200

7c,2

007f

).

278

Tabl

eC

.6Pr

ojec

ted

dis

trib

uti

onof

tota

lh

ealt

hex

pen

dit

ure

(Rs.

mil

lion

)

Yea

rC

urr

ent

situ

atio

nP

rop

ose

dp

rogr

amm

e

Tota

lO

OP

hea

lth

exp

.in

cl.

5%C

AG

R

Est

imat

edto

tal

hea

lth

exp

.(T

HE

)

Pu

bli

ch

ealt

hex

p.(

PH

E)

Tota

lO

OP

hea

lth

exp

.G

DP

esti

mat

esP

HE

as%

of

GD

P

−72%

−100

%62

.83%

37.1

7%

2006

853,

273

1,18

5,10

174

4,55

144

0,55

139

,743

,850

1.87

2007

912,

886

1,26

7,89

879

6,56

847

1,32

945

,453

,590

1.75

2008

976,

783

1,35

6,64

385

2,32

350

4,32

050

,916

,870

1.67

2009

1,04

5,96

71,

452,

731

9,12

6,92

540,

040

57,3

61,8

801.

5920

101,

118,

570

1,55

3,57

09,

760,

4557

7,52

564

,612

,270

1.51

2011

1,19

3,73

71,

657,

968

1,04

1,63

461

6,33

472

,713

,230

1.43

2012

1,27

3,98

41,

769,

422

1,11

1,65

665

7,76

781

,814

,440

1.36

2013

1,35

9,36

01,

888,

000

1,18

6,15

370

1,84

692

,075

,660

1.29

2014

1,44

9,16

42,

012,

728

1,26

4,51

574

8,21

310

3,58

5,11

81.

2220

151,

544,

667

2,14

5,37

11,

347,

849

797,

522

116,

533,

257

1.16

Sour

ce:A

uth

ores

tim

ates

base

don

GO

I(2

005b

,200

7c);

and

IMF

(200

8).

Appendix D

Sensitivity test: Case 2

Co-payment for the lowest income category is raised to Rs. 15 and Safety Netthreshold raised to Rs. 750. The payment schedule for the other categoriesremains unchanged.

279

280

Tabl

eD

.1En

titl

emen

tsof

Ind

iaH

ealt

hca

rds

ata

glan

ce

S.N

oIn

com

ep

.a.

Cat

ego

ryC

olo

ur

Co

-pay

men

tp

erp

resc

rip

tio

nSa

fety

Net

Th

resh

old

Co

-pay

men

t(p

ost

Safe

tyN

et)

per

pre

scri

pti

on

(Rs.

)(R

s.)

(Rs.

)(R

s.)

1N

one

S-C

ard

Bro

wn

Nil

N.A

.N

il2

<15

,000

B1-

Car

dR

edN

ilN

.AN

il3

15,0

01–4

0,00

0B

2-C

ard

Yell

ow15

750

Nil

415

,001

–40,

000

A1-

Car

dW

hit

e/Ye

llow

1575

0N

il5

40,0

01–1

00,0

00A

2-C

ard

Wh

ite/

Purp

le25

1125

156

40,0

01–1

00,0

00M

1-C

ard

Purp

le25

1125

157

>10

0,00

0A

3-C

ard

Wh

ite/

Gre

en50

2000

258

>10

0,00

0M

2-C

ard

Gre

en50

2000

25

Not

e:T

he

thre

shol

dw

ould

kick

inat

40p

resc

rip

tion

sfo

rB

2an

dA

1C

ateg

orie

s,at

45p

resc

rip

tion

sfo

rM

1an

dA

2ca

tego

ries

,an

dat

50p

resc

rip

tion

sfo

rM

2an

dA

3ca

tego

ries

.So

urce

:Au

thor

.

281

Tabl

eD

.2C

alcu

lati

ng

hea

lth

and

med

icin

eex

pen

dit

ure

(Rs.

)

Cat

ego

ryP

op

ula

tio

n(M

illi

on

)H

ealt

h(m

on

thly

)M

edic

ine

(mo

nth

ly)

Ind

ia11

40P

erca

pit

a(R

s.)

Tota

lR

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Notes

2 The WTO and the TRIPS Agreement

1. Pharmaceutical sector inquiry: Preliminary report submitted on 28 November2008 found up to 1300 patents filed EU-wide on a single medicine. We havetermed this act as excessive patenting.

3 The Global Pharmaceutical Industry andDeveloping New Drugs

1. Product with annual sales of more than a billion dollars.2. According to Pammolli and Riccaboni (2007), the off-shoring of manufacture

by the US pharmaceutical firms increased five times between 1996 and 2004.

4 Development of India’s Pharmaceutical Industry

1. Certain drugs are reserved for manufacture by the SSI, for which to qualify,the total outlay must not exceed Rs. 10 million ($222,000). This limit iscurrently in the process of being increased to Rs. 50 million ($1.15 million).

2. The actual drug or salt used in the formulation (e.g. the drug Paracetamolused in Panadol).

3. Filed to obtain approvals for bulk drugs.4. Filed to obtain approvals for generic versions of formulations.5. No breakdown of the export value of each drug was available separately. The

value of the whole item was used in calculation.6. Item no. 211 had four drugs, of which patents on all but paclitaxel had

expired. Paclitaxel is a natural molecule, thus a product patent would notbe applicable to it per se. However, considering that a patent on its ‘methodof working’ exists in South Africa till 2013, the whole item was included inthe examination, as its export may be affected by the new patent regime inIndia.

7. Foreign Exchange Regulation Act (FERA).8. The significance of this period is that it covers the period of restrictive mea-

sures of the 1970s as well as the period following economic reforms in1991.

9. For the years obtained from the IMF database and average for each periodderived.

10. The FDI confidence index was not available for 2006.

5 TRIPS and the Indian Patents Regime

1. The High Court is the highest court in a state/province. The Supreme Court isthe apex court of India.

286

Notes 287

2. Defined as mastering the ability to read patents ‘in such a way that you canbypass someone’s invention’, and ‘to write patents in such a way that nobodycan bypass you’ (Mashelkar 2003).

3. Indian Network for People Living with HIV/AIDS, the Manipur Network ofPositive People, and the Lawyers Collective.

4. (Chapter XVI, Section 84(1)).5. As noted earlier, Roche has a patent on Taraceva in India.

6 Price Controls and Drug Affordability in India:Policy Options

1. Author calculations based on CIMS (2007).2. List of drugs under price control.3. Under Section (2) of the Essential Commodities Act, medicines are consid-

ered essential commodities.4. As listed in Schedule – I appended to the DPCO – 1970.5. Transfer pricing refers to companies charging their subsidiary significantly at

a higher price for a product than otherwise available.6. The All India Drug Action Network (AIDAN), the Medico Friends Circle

(MFC), the Low Cost Standard Therapeutics (LOCOST), and the Jan SwasthyaSahyog.

7. The 354 drugs on the NLEM list minus the 15 drugs currently under pricecontrol.

8. Dispensed as received, that is without breaking the packs or taking out smallquantities from bottles and so on.

9. CIMS, Drug Today, and IDR are the reference books used by medicalpractitioners to prescribe medicines.

10. Uttar Pradesh is the most populous state in India.11. Emails to Sakthivel were not replied. (on record with the author).12. Email from the TGA on record with the author.

7 Health Insurance in India

1. The Union Government contributes 75 per cent and the states 25 per cent.2. Organisation for Economic Co-operation and Development.3. Denotes holders of a Pensioner Concession Card; Australian Seniors

Health Card; Health Care Card; or DVA White, Gold, or Orange Card.(http://www.pbs.gov.au/html/consumer/pbs/about). These cards are meanstested, which means that people with assets above the government thresholdwould be ineligible.

8 Broadening Access to Medicines andHealthcare in India

1. While the official estimates suggest 233 million population lives below thepoverty line in India, experts such as Patnaik (2010) find considerable dis-crepancies and inconsistencies in the methodology used in the estimates and

288 Notes

claim the actual figure to be significantly higher. Our estimate of 350 millionfor the BPL population may be closer to reality.

2. The expression used in drug evaluation literature.3. The yoga practitioners would be excluded for two reasons. First, under yogic

therapies, no medicine is dispensed. The main focus is on physical exercisesand body postures. Two, there is no framework in place for validation of theyogic claims or for qualifications.

4. Includes the Department of Veterans Affairs-issued Pensioner ConcessionCards and Commonwealth Seniors Health Cards. The Department of HumanServices through Centrelink also issues a range of Health Care Cards andother types of concession cards, such as Disability Support Pension Card.

5. Consumer Price Index.6. Wholesale Price Index used in India.7. Over the age of 65 years.8. Adjusted up from 1991 figures of 38.8 million for disabled in Government of

India (2003b, p. 98).9. Under the proposal, the year would mean Indian accounting year (April–

March) because it would be easier for budgetary planning and accountingpurposes.

10. Medicines specifically listed under the 20-day Rule (e.g. for chronic diseasessuch as HIV/AIDS).

11. Based on Government of India (2007f).12. Total out-of-pocket payments/total number of IndiaHealthcards.13. Rs. 141,419/150 (sum of all cards except S and B1 categories).14. Employees’ State Insurance Scheme (ESIS).15. Central Government Health Scheme (CGHS).

9 Is TRIPS Appropriate for Developing Countries?

1. The German Parliament until 1945.2. It is assumed that each product would have identical demand functions.3. Oxfam (2002) estimates, the poor countries would contribute $40 billion

annually in TRIPS-inflicted additional costs.4. Deliberate use of this figure rather than the recent estimates of $1.3 billion,

because the actual outlay is less than half of the new estimates and thedeveloping countries would be actually paying additional costs.

5. See Chapter 5 for more details.6. Rector, Imperial College, London.

10 Which Way Ahead?

1. Around 100 world’s largest pharmaceutical companies based in the US, EU,and Japan.

2. Such as 1300 patents on a single drug noted earlier in the chapter.

References

A T Kearney 2004, ‘FDI Confidence Index’, Global Business Policy Council, vol. 7,October.

———2005, ‘FDI Confidence Index’, Global Business Policy Council, vol. 8,December.

———2007, New Concerns in an Uncertain World: The 2007 A.T. Kearney ForeignDirect Investment confidence index, Global Business Policy Council, Vienna, VA.

Abbott, FM 1998, ‘The enduring enigma of TRIPS: A challenge for the world eco-nomic system’, Journal of International Economic Law, vol. 1, no. 4, pp. 497–521.

———2003, The Competition Provisions in the TRIPS Agreement: Implications forTechnology Transfer, Paper presented to WIPO–WTO Joint Workshop: Intellec-tual Property Rights and Transfer of Technology, Geneva, 17 November.

———2005, ‘The WTO medicines decision: World pharmaceutical trade and theprotection of pubic health’, American Journal of International Law, vol. 99, no. 2,pp. 317–58.

Abegunde, D & Stanciole, A 2006, ‘An estimation of the economic impactof chronic noncommunicable diseases in selected countries’, Working paper,World Health Organization, Geneva, 30 May, viewed 23 January 2009,http://www.who.int/chp/working_paper_growth%20model29may.pdf.

Acharya, A & Ranson, MK 2005, ‘Health care financing for the poor: Community-based health insurance schemes in Gujarat’, Economic and Political Weekly,vol. 40, no. 38, pp. 4141–50.

Aderibigbe, MR 1990, ‘The Nigerian patent system and the new industrial policy’,World Patent Information, vol. 12, no. 2, pp. 95–9.

Adikibi, OT 1988, ‘The multinational corporation and monopoly of patents inNigeria’, World Development, vol. 16, no. 4, pp. 511–26.

Aggarwal, A 2004, ‘Strategic approach to strengthening the international compet-itiveness in the knowledge based industries: The Indian pharmaceutical indus-try’, Discussion paper RIS-DP # 80/2004, Research and Information System forthe Non-Aligned and Other Developing Countries, New Delhi.

Ahuja, R & Narang, A 2005, ‘Emerging trends in health insurance for low-incomegroups’, Economic and Political Weekly, vol. 40, no. 38, pp. 4151–7.

Aiyer, S 2006, ‘Indian MNCs: Indian companies hunt for assets abroad to acquireglobal scale’, India Today, vol. 31, no. 44, pp. 38–48.

Alexander, J 2007, ‘ICMR launches medical innovation fund to support novelinitiative in drug research’, Pharmabiz, 20 February.

Alsegård, E 2004, ‘Global pharmaceutical patents after the Doha Declaration:What lies in the future?’, SCRIPT-ed, vol. 1, no. 1, 23 February.

Angell, M 2004, The Truth About the Drug Companies: How They Deceive Us andWhat To Do About It, Random House, New York.

Ashton, TS 1964, The Industrial Revolution: 1760–1830, Oxford University Press,London, UK.

289

290 References

Australian Bureau of Statistics 2006, ‘Population projections, Australia, 2004to 2101’, viewed 23 June 2008, http://www.abs.gov.au/ausstats/[email protected]/ProductsbyCatalogue/5A9C0859C5F50C30CA25718C0015182F?OpenDocument.

Australian Institute of Health and Welfare 2005, Health system expenditure on dis-ease and injury in Australia, 2000–01, Health and Welfare expenditure seriesno. 21, 2nd edn, Canberra.

Austrom, D & Howard, P 1994, ‘Speeding drugs to market: Strategies forre-engineering’, Scrip Magazine, October, pp. 50–2.

Babu, G 2007, ‘Cadila Pharma to launch SEZ in the third quarter of 2008’,Pharmabiz, 11 May.

Baker, BK 2008, ‘Ending drug registration apartheid: Taming data exclusivityand patent/registration Linkage’, American Journal of Law & Medicine, vol. 34,no. 2/3, pp. 303–44.

Balasubramaniam, K 2002, ‘Access to medicines: Patents, prices and public pol-icy – consumer perspectives’, in P Drahos & R Mayne (eds), Global IntellectualProperty Rights: Knowledge, Access and Development, Palgrave Macmillan, NewYork, pp. 90–107.

Ballance, R, Pogány, J & Forstner, H 1992, The World’s Pharmaceutical Industries:An International Perspective on Innovation, Competition and Policy, United NationsIndustrial Development Organization and Edward Elgar Publishing, Aldershot,England.

Barry, M 2003, ‘Presidential address: Diseases without borders – Globalization’schallenge to the American society of tropical medicine and hygiene: A call forpublic advocacy and activism’, The American Journal of Tropical Medicine andHygiene, vol. 69, no. 1, pp. 3–7.

Barton, J 2001, ‘Differentiated pricing of patented products’, rev. edn, Work-ing paper no. 63, Indian Council for Research on International EconomicRelations, New Delhi, November.

———2003, Preserving the Global Scientific and Technological Commons, Paperpresented to Science and Technology Diplomacy Initiative and the ICTSD-UNCTAD Project on IPRs and Sustainable Development Policy Dialogue on aProposal for an International Science and Technology Treaty, Room 25, Palaisdes Nations, Geneva, 11 April, viewed 23 February 2006, http://stdev.unctad.org/capacity/Barton.doc.

Barton, JH & Maskus, KE 2004, ‘Economic perspectives on a multilateral agree-ment on open access to basic science and technology’, SCRIPT-ed, vol. 1, no. 3,pp. 367–87.

Berndt, ER, Glennerster, R, Kremer, MR, Lee, J, Levine, R & Weizsäcker, G2005, ‘Advanced purchase commitments for a malaria vaccine: Estimatingcosts and effectiveness’, Discussion paper no. PEPP/2, Suntory and ToyotaInternational Centres for Economics and Related Disciplines, London Schoolof Economics and Political Science, London, April, viewed 14 March 2006,http://sticerd.lse.ac.uk/dps/pepp/pepp02.pdf.

Berry, A 2005, ‘Third-world medicine: A new way of developing drugs forneglected diseases of the poor world’, The Economist, 14 April.

Bhagat, M 1982, Aspects of Drug Industry in India, Centre for Education andDocumentation, Bombay.

References 291

Bidwai, P 2007, ‘Novartis patents case far from dead’, Transnational Insti-tute, viewed 3 December 2008, http://www.tni.org/detail_page.phtml?act_id=17188.

Bisserbe, N 2006, ‘It’s jungle out there’, Economic Times, 15 October.Blech, J 2006, Inventing Disease and Pushing Pills: Pharmaceutical Companies and

the Medicalisation of Normal Life, Routledge, London and New York.Blendon, RJ, Schoen, C, DesRoches, CM, Osborn, R, Scoles, KL & Zapert, K 2002,

‘Inequities in health’, Health Affairs, vol. 21, no. 3, pp. 182–91.Bloomberg 2006, ‘Pfizer investors to suffer from halting of Lipitor replace-

ment: Big M&A to come?’, Seeking Alpha, no. 4, December, viewed27 January 2009, http://seekingalpha.com/article/21659-pfizer-investors-to-suffer-from-halting-of-lipitor-replacement-big-m-a-to-come.

Boldrin, M & Levine, D 2005, The Pharmaceutical Industry, University ofCalifornia, viewed 23 February 2006, http://levine.sscnet.ucla.edu/papers/ip.ch.9.m1004.pdf.

Bower, DJ & Sulej, JC 2007, ‘The Indian challenge: The evolution of a success-ful new global strategy in the pharmaceutical industry’, Technology Analysis &Strategic Management, vol. 19, no. 5, pp. 611–24.

Braee, R 2001, New Zealand Pharmaceutical Pricing and Reimbursement Policies,European Commission, Brussels.

Brown, P 2004, ‘Fiddling with prices’, Scrip Magazine, June, pp. 3–4.Bureau of National Affairs 2001, ‘Rewriting TRIPS could hurt research: Pharma-

ceutical industry strongly warns WTO’, WTO Reporter, 20 September.Cai, Q & Salmon, JW 2005, ‘What role may pharmaeconomics play in phar-

maceutical pricing and reimbursement in China?’, Journal of PharmaceuticalFinance, Economics & Policy, vol. 14, no. 1, pp. 51–75.

Caplow, T, Hicks, L & Wattenberg, B 2006, The First Measured Century, PublicBroadcasting Services, Arlington, VA, viewed November 2006, http://www.pbs.org/fmc/book/2work4.htm.

Central Drug Research Institute (CDRI) 2008, New Drugs, Central DrugResearch Institute, Lucknow, viewed 12 April 2008, http://www.cdriindia.org/newdrugs.htm.

Chadha, A 2006, ‘Destination India for the pharmaceutical industry’, The DelhiBusiness Review, vol. 7, no. 1, pp. 1–8.

Chataway, J, Tait, J & Wield, D 2007, ‘Frameworks for pharmaceutical innova-tion in developing countries: The case of Indian pharma’, Technology Analysis& Strategic Management, vol. 19, no. 5, pp. 697–708.

Chataway, M 2000, ‘A radical idea for how pharma can help the developingworld’, Scrip Magazine, October, pp. 21–5.

Chaturvedi, K 2005, ‘Policy and technology co-evolution in the Indian phar-maceutical industry’, DPP Working paper no. 50, Development Policy andPractice, Faculty of Technology, The Open University, Walton Hall, MiltonKeynes, December.

Chaudhuri, S 2005, The WTO and India’s Pharmaceutical Industry: Patent Protection,TRIPS and Developing Countries, Oxford University Press, New Delhi.

Chaudhuri, S, Goldberg, P & Jia, P 2003, ‘The effects of extending intellec-tual property rights protection to developing countries: A case study of theIndian pharmaceutical market’, Working paper no. 10159, National Bureau ofEconomic Research, Cambridge, MA, December.

292 References

Chin, J & Grossman, G 1990, ‘Intellectual property rights and north-southtrade’, in RW Jones & AO Krueger (eds), The Political Economy of InternationalTrade: Essays in Honor of Robert E. Baldwin, Basil-Blackwell, Cambridge, MA,pp. 90–107.

CIMS 2007, CIMS, vol. 98, no. 3, Bio Gard Publishers, Bangalore, July–October.Cipla 2005, Annual Report 2004–05, Cipla Pharmaceuticals, Mumbai.———2008, Annual Report 2007–08, Cipla Pharmaceuticals, Mumbai.Clements, PJ 2007–08, ‘The Hatch-Waxman Act and the conflict between

antitrust law and patent law’, IDEA: The Intellectual Property Law Review, vol. 48,no. 3, pp. 381–407.

Clift, C 2007, ‘Data protection and data exclusivity in pharmaceuticals and agro-chemicals’, in A Krattiger, RT Mahoney, L Nelsen, JA Thomson, AB Bennett,K Satyanarayana, GD Graff, C Fernandez and SP Kowalski (eds), IntellectualProperty Management in Health and Agricultural Innovation: A Handbook of BestPractices, MIHR, Oxford, UK and PIPRA, Davis, USA, vol. 2.

Cole, JH 2001, ‘Patents and copyrights: Do the benefits exceed the costs?’, Journalof Libertarian Studies, vol. 15, no. 4, pp. 79–105.

Collier, R 2009, ‘Drug development cost estimates hard to swallow’, CanadianMedical Association Journal, vol. 180, no. 3, 3 February.

Commission on Intellectual Property Rights 2002, ‘Integrating intellectual prop-erty rights and development policy’, London, September, viewed 5 June 2005,http://www.iprcommission.org/papers/pdfs/final_report/CIPRfullfinal.pdf.

Commission on Intellectual Property Rights Innovation and Public Health2006, Public Health: Innovation and Intellectual Property Rights, World HealthOrganization, Geneva.

Commission on Macroeconomics and Health 2001, Macroeconomics and Health:Investing in Health for Economic Development, World Health Organization,Geneva.

Congressional Budget Office (CBO) 1998, Pricing and Competition in the Phar-maceutical Market: How Increased Competition from Generic Drugs Has AffectedPrices and Returns in the Pharmaceutical Industry, Congressional Budget Office,Government of the United States, Washington, DC.

Cornish, WR 1989, Intellectual Property: Patents, Copyrights, Trademarks and AlliedRights, Sweet and Maxwell, London.

Correa, CM 2002a, ‘Pro-competitive measures under TRIPS to promote tech-nology diffusion in developing countries’, in P Drahos and R Mayne (eds),Global Intellectual Property Rights: Knowledge, Access and Development, PalgraveMacmillan, New York, pp. 40–60.

———2002b, ‘Unfair competition under the TRIPS agreement: Protection ofdata submitted for the registration of pharmaceuticals’, Chicago Journal ofInternational Law, vol. 3, no. 1, pp. 69–86.

———2006, ‘Implications of bilateral free trade agreements on access tomedicines’, Bulletin of the World Health Organization, vol. 84, no. 5, pp. 399–404.

Cruddas, J & Gannon, Z 2009, A bitter pill to swallow: Drugs for people not justfor profit, Compass, London, 26 August.

Cutler, DM 2007, ‘The demise of the blockbuster?’, The New England Journal ofMedicine, vol. 356, no. 13, pp. 1292–3.

Cygnus 2005, Industry Insight: Indian Pharmaceuticals, Cygnus Business Consult-ing & Research, Hyderabad.

References 293

———2007, Quarterly Performance Analysis of Companies (October–December 2006):Indian Pharmaceutical Industry, Cygnus Business Consulting & Research,Hyderabad.

Danzon, P 2001, Differential Pricing: Reconciling R&D, IP and Access, paperpresented to WHO/WTO Workshop on Differential Pricing and Financ-ing of Essential Drugs, Hosbjor, Norway, 8–11 April, viewed 14 October2004, http://www.wto.org/english/tratop_e/trips_e/hosbjor_presentations_e/12danzon_e.pdf.

Danzon, PM, Epstein, A & Nicholson, S 2007, ‘Mergers and acquisitions in thepharmaceutical and biotech industries’, Managerial and Decision Economics,vol. 28, no. 4–5, pp. 307–28.

Darbourne, A 2003, ‘Access to medicines: Worlds apart’, Scrip Magazine, February,pp. 36–8.

Das, SC, Mandal, M & Mandal, SC 2007, ‘A critical study on availability andprice variation between different brands: Impact on access to medicines’, IndianJournal of Pharmaceutical Sciences, vol. 69, no. 1, pp. 160–3.

David, P 1993, ‘Intellectual property institutions and the panda’s thumb: Patents,copyrights, and trade secrets in economic theory and history’, in M Wallerstein,M Mogee and R Schoen (eds), Global Dimensions of Intellectual Property Rights inScience and Technology, National Academy Press, Washington, DC, pp. 19–61.

Davis, M 1994, ‘Patents in healthcare: Subsidy and victimisation?’, Scrip Magazine,December, pp. 6–8.

Deardof, A 1992, ‘Welfare effects of global patent protection’, Economica, vol. 59,no. 233, pp. 35–51.

Deloitte Recap 2009, ‘Biotech database’, Deloitte Recap LLC, viewed 28 January2009, http://www.deloitte.com/.

DeNavas-Walt, C, Proctor, BD & Smith, J 2007, Income, Poverty, and Health Insur-ance Coverage in the United States: 2006, US Census Bureau, U.S Department ofCommerce, Economics and Statistics Administration.

Department of Health 2005, ‘Reimbursement of “standard” branded genericmedicines: A further consultation’, viewed 17 July 2007, http://www.dh.gov.uk/en/Consultations/Closedconsultations/DH_4121799.

DiMasi, JA 1991, The Cost of Innovation in the Pharmaceutical Industry:New Drug R&D Cost Estimates, Pharmaceutical Manufacturers Association,Washington, DC.

———2001, ‘New drug development in the United States from 1963 to 1999’,Clinical Pharmacology & Therapeutics, vol. 69, no. 5, May, pp. 286–96.

DiMasi, JA & Grabowski, HG 2007, ‘The cost of biopharmaceutical R&D:Is biotech different?’, Managerial and Decision Economics, vol. 28, no. 4–5,pp. 469–79.

DiMasi, JA, Hansen, RW & Grabowski, HG 2003, ‘The price of innovation: Newestimates of drug development costs’, Journal of Health Economics, vol. 22, no. 2,pp. 151–85.

Dongre, RCK 1982, Shrimad Bhagwad-Rahasya [The Secret of God], MaanasPrakashan, New Delhi.

Dr Reddy’s 2004, ‘Address by Dr. K Anji Reddy’, Pharmacophore 2004, Inter-national Symposium, Innovating Drugs: Emerging Perspectives, Hyderabad,16–17 January, viewed 10 January 2006, http://www.drreddys.com/coverview/pdf/speeches/Pharmacophore2004_address.pdf.

294 References

———2005, Annual Report 2004–2005, Dr Reddy’s Labs, viewed 15 September2005, http://www.drreddys.com/investors/pdf/annualreport2005.pdf.

———2008, ‘API-product list’, viewed 18 September 2008, http://www.drreddys.com/gchemicals/api_productlist.htm.

Drahos, P 2002a, ‘Introduction’, in P Drahos & R Mayne (eds), Global IntellectualProperty Rights: Knowledge, Access and Development, Palgrave Macmillan, NewYork, pp. 1–12.

———2002b, ‘Negotiating intellectual property rights: Between coercion anddialogue’, in P Drahos & R Mayne (eds), Global Intellectual Property Rights:Knowledge, Access and Development, Palgrave Macmillan, New York, pp. 161–82.

Drahos, P & Braithwaite, J 2002, ‘Intellectual property, corporate strategy, glob-alisation: TRIPS in context’, Wisconsin International Law Journal, vol. 20, no. 3,pp. 451–80.

Drahos, P, Faunce, T, Goddard, M & Henry, D 2004, ‘The FTA and the PBS:A Submission to the Senate Select Committee on the US-Australia Free TradeAgreement’, Government of Australia, Canberra.

Drahos, P 2008, ‘ “Trust me”: Patent offices in developing countries’, AmericanJournal of Law & Medicine, vol. 34, no. 2, pp. 151–74.

Drohan, M 1996, ‘Canada can take heart from earlier WTO ruling: Backgrounderfor countries in danger of being pushed around by large neighbours, decisionbacking Venezuela over U.S. was special’, The Globe and Mail, 13 March, p. A12.

Drug Today 2005, Drug Today, vol. 12, no. 3, January–March.———2007, Drug Today, vol. 15, no. 2, October–December.Duckett, SJ 2004, ‘Drug policy down under: Australia’s Pharmaceutical Benefits

Scheme’, Health Care Financing Review, vol. 25, no. 3, pp. 55–67.Dukes, G 2006, The Law and the Ethics of the Pharmaceutical Industry, Elsevier,

Amsterdam.Dunkley, G 2001, The Free Trade Adventure: The Uruguay Round and Globalism –

A Critique, Melbourne University Press, Melbourne.Dutta, A 2005, ‘Free entry in the market for drugs in India: Implications for social

welfare’, MIT, viewed 22 February 2006, http://econ-www.mit.edu/graduate/candidates/download_res.php?id=254.

Economic Research Foundation 2006, ‘Government health expenditure in India:A benchmark study undertaken for the MacArthur Foundation’, viewed 1 July2008, http://www.macroscan.org/anl/oct06/pdf/Health_Expenditure.pdf.

EFPIA 2006, The Pharmaceutical Industry in Figures, European Federation of Phar-maceutical Industries and Associations, Brussels, viewed 22 November 2006,http://www.efpia.org/6_publ/infigures2006.pdf.

———2008, The Pharmaceutical Industry in Figures, European Federation ofPharmaceutical Industries and Associations, Brussels, viewed 3 August 2008,http://www.efpia.eu/Content/Default.asp?PageID=559&DocID=4883.

Elliott, R 2008, Delivery Past Due: Agreement Between Rwanda and Canadian GenericPharmaceutical Company Represents Historic First Use of WTO Rules on CompulsoryLicensing For Export, But Could Be Last, Paper presented to XVII Interna-tional AIDS Conference, Mexico City, 3–8 August, viewed 2 January 2008,http://www.aids2008.org/Pag/Abstracts.aspx?SID=290&AID=15940.

Ellis, RP, Alam, M & Gupta, I 2000, ‘Health insurance in India: Prognosis andprospectus’, Economic and Political Weekly, vol. 35, no. 4, pp. 207–17.

References 295

Embassy of the United States 2008, ‘IPR toolkit India: Patents’, viewed 28 October2008, http://newdelhi.usembassy.gov/iprpatents.html.

Essentialdrugs 2004, ‘India-drug: Total number of drug units in India’, Essen-tial Drugs, viewed 5 October 2004, http://www.essentialdrugs.org/indiadrug/archive/200401/msg00032.php.

EurActiv 2005, ‘Review of EU pharmaceutical legislation’, 11 February, viewed12 December 2008, http://www.euractiv.com/en/health/new-medicines-legislation/article-117531.

European Commission 2008, Pharmaceutical Sector Inquiry: PreliminaryReport, European Commission, Brussels, 28 November, viewed 10 Decem-ber 2008, http://ec.europa.eu/comm/competition/sectors/pharmaceuticals/inquiry/preliminary_report.pdf.

European Generic Medicines Association 2007, ‘Generic market shares acrossEurope in 2006’, viewed 5 July 2007, http://www.egagenerics.com/doc/fac-GxMktEur_2006.pdf.

European Parliament 2007, ‘Written declaration’, 0022/2007, 26 February,viewed 13 January 2009, http://www.europarl.europa.eu/sides/getDoc.do?pubRef=-//EP//NONSGML+WDECL+P6-DCL-2007-0022+0+DOC+PDF+V0//EN&language=EN.

Federal Trade Commission 2003, ‘To Promote Innovation: The Proper Balance ofCompetition and Patent Law and Policy’, Washington, DC, 28 October, viewed15 October 2008, http://www.ftc.gov/opa/2003/10/cpreport.shtm.

Ferreiro, A 2000, ‘Private health insurance in India: Would its implementationaffect the poor?’, in D Peters, GNV Ramana & KS Rao (eds), Private Health Insur-ance and Public Health Goals in India: Report on a National Seminar, World Bank,New Delhi, pp. 79–83.

FICCI 2005, Competitiveness of the Indian Pharmaceutical Industry in the NewProduct Patent Regime: FICCI Report for National Manufacturing Competi-tiveness Council (NMCC), Federation of Indian Chambers of Commerce andIndustry, New Delhi.

———2007, ‘Govt to Frame India Innovation Act to Spur Research and Innova-tion: Kapil Sibal’, Federation of Indian Chambers of Commerce and Industry,New Delhi.

FierceBiotech 2006, ‘Dr. Reddy’s to buy betapharm in $570M deal’,viewed 3 February 2007, http://www.fiercebiotech.com/story/dr-reddy-s-to-buy-betapharm-in-570m-deal/2006-02-16.

Finger, JM 2002, ‘Implementing the Uruguay Round Agreements’, in P Lloyd &C Milner (eds), The World Economy: Global Trade Policy 2001, Blackwell Publish-ing, Oxford, UK, pp. 7–18.

Finger, JM & Schuler, P 2001, ‘Implementation of Uruguay round commit-ments: The development challenge’, World Bank Policy Research Workingpaper no. 2215, World Bank, Washington DC, viewed 23 June 2003, http://econ.worldbank.org/external/default/main?ImgPagePK=64202990&entityID=000094946_01013005324822&pagePK=64210502&theSitePK=544849&piPK=64210520.

Flink, JJ 1990, ‘Henry Ford and the triumph of the automobile’, in W Caroll &J Pursell (eds), Technology in America: A History of Individuals and Ideas, MIT Press,Cambridge, MA.

296 References

Food and Drug Administration (FDA) 2008, Electronic Orange Book: Approved DrugProducts with Therapeutic Equivalence Evaluations, Food and Drug Administra-tion, Government of the United States of America, viewed 2 December 2008,http://www.fda.gov/cder/ob/docs/querytn.htm.

Foroohar, R 2006, ‘A new drug deal’, Newsweek, December 2005–February 2006,p. 78.

Frank, R & Hensley, S 2002, ‘Pfizer to buy Pharmacia for $60 billion in stock’, TheWall Street Journal, 15 July, p. 1.

Galpalli, N 2004, ‘GATT agreement: Effect on drug prices in India’,Pharmainfo.net, viewed 18 February 2005, http://pharmainfo.net/subjects-viewpage-pageid-82.html.

Gambardella, A 1995, Science and Innovation: The US Pharmaceutical IndustryDuring the 1980s, Cambridge University Press, New York.

Gambardella, A, Orsenigo, L & Pammolli, F 2000, Global Competitiveness inPharmaceuticals: A European Perspective, Report Prepared for the DirectorateGeneral Enterprise of the European Commission, Brussels.

Garg, CC 2000, ‘Implications of current experiences of health insurance in India’,in D Peters, GNV Ramana & KS Rao (eds), Private Health Insurance and PublicHealth Goals in India: Report on a National Seminar, World Bank, New Delhi,pp. 3–42.

Gassmann, O, Reepmeyer, G & von Zedtwitz, M 2004, Leading PharmaceuticalInnovation: Trends and Drivers for Growth in the Pharmaceutical Industry, Springer-Verlag, Berlin.

———2008, Leading Pharmaceutical Innovation: Trends and Drivers for Growth inthe Pharmaceutical Industry, 2nd edn, Springer-Verlag, Berlin.Gehl Sampath, P2006, ‘India’s product patent protection regime: Less or more of “Pills for thePoor”?’, The Journal of World Intellectual Property, vol. 9, no. 6, pp. 694–726.

Genepharm 2005, Annual Report, Genepharm Australasia, Melbourne.General Insurance Corporation of India 2008, ‘History in brief’, viewed 9 July

2008, http://gicofindia.in/en/.Generic Handbook 2007, Generic Handbook, 2nd edn, VOI Consulting, New

Orleans.Global-Challenges 2008, ‘AIDS: Third world: 1999–2008: Global issues of the

twenty-first century and United Nations challenges’, viewed 20 September2008, http://www.global-challenges.org/30aids-thirdworld.html.

Global Forum for Health Research 1999, ‘The 10/90 report on health research’,Global Forum for Health Research, Geneva, viewed 4 January 2009, http://www.globalforumhealth.org/filesupld/1090_report_99/99ex_summary.PDF.

———2004, The 10/90 Gap in Health Research, Global Forum for Health Research,Geneva, viewed 4 January 2009, http://www.globalforumhealth.org/filesupld/1090_report_03_04/109004_chap_5.pdf.

Goddard, M, Hauck, K, Preker, A & Smith, PC 2006, ‘Priority setting in health: Apolitical economy perspective’, Health Economics, Policy and Law, vol. 1, no. 1,pp. 79–90.

Goozner, M 2004, The $800 Million Pill: The Truth Behind the Cost of New Drugs,University of California, Berkeley and Los Angeles, CA.

Government of Australia 2006, Expenditure and Prescriptions Twelve Months to 30June 2006, Department of Health and Ageing, Canberra, Australia.

References 297

———2007a, Australian Regulation of Prescription Medical Products, Ther-apeutic Goods Administration, Department of Health and Ageing,Canberra.

———2007b, Pharmaceutical Benefits Scheme (PBS) Reform, Therapeutic GoodsAdministration, Department of Health and Ageing, Canberra.

———2008, ‘What is intellectual property? an introduction to intellec-tual property’, viewed 10 December 2008, http://www.ipaustralia.gov.au/ip/introduction.shtml.

———2010, Overview of the PBS Safety Net?, Medicare Australia, Canberra, viewed27 January 2010, http://www.medicareaustralia.gov.au/public/services/scripts/pbs.jsp.

Government of Canada 2008, How Does the PMPRB Review the Pricing Infor-mation For All Patented Medicines Sold in Canada?, Patented Medicine PricesReview Board, Ottawa, viewed 27 August 2008, http://www.pmprb-cepmb.gc.ca/english/view.asp?x=272#16.

Government of India (GOI) 1952, First Five-Year Plan (1952–57), Planning Com-mission of India, New Delhi.

———1957, Second Five-Year Plan (1957–1962), Planning Commission of India,New Delhi.

———1972, The Patent Act 1970, Office of the Controller General of Patents,Designs and Trade Marks, Kolkata.

———1977, Drug Policy – 1977, Department of Chemicals and Petrochemicals,Ministry of Chemicals and Fertilizers, New Delhi.

———1980, Sixth Five-Year Plan (1980–85), Planning Commission of India, NewDelhi.

———1986, Drug Policy – 1986, Department of Chemicals and Petrochemicals,Ministry of Chemicals and Fertilizers, New Delhi.

———1994, Drug Policy – 1994, Department of Chemicals and Petrochemicals,Ministry of Chemicals and Fertilizers, New Delhi.

———1995, Drugs (Price Control) Order 1995, Department of Chemicals andPetrochemicals, Ministry of Chemicals and Fertilizers, Government of India,New Delhi.

———1999, The Patents (Amendment) Act, 1999, no. 17 of 1999, 26 March 1999,http://ipindia.nic.in/ipr/patent/patact_99.PDF.

———2002a, National Health Policy – 2002, Ministry of Health and FamilyWelfare, Government of India, New Delhi.

———2002b, The Patents (Amendment) Act, 2002, no. 38 of 2002, 25 June 2002,http://ipindia.nic.in/ipr/patent/patentg.pdf.

———2002c, Pharmaceutical Policy – 2002, Press Information Bureau, Govern-ment of India, viewed 16 January 2003, http://pib.nic.in/archive/Ireleng/Iyr2002/rfeb2002/15022002/r1502200212.html.

———2002d, Pharmaceutical Policy – 2002, Department of Chemicals andPetrochemicals, Ministry of Chemicals and Fertilizers, New Delhi.

———2003a, Functions of NPPA, National Pharmaceutical Pricing Authority,Government of India, New Delhi.

———2003b, Health Information of India 2000 & 2001, Central Bureau of HealthIntelligence, Directorate General of Health Services, Ministry of Health &Family Welfare, New Delhi.

298 References

———2003c, Statistical Pocket Book – India 2002, Central Statistical Organisation,Ministry of Statistics and Programme Implementation, New Delhi.

———2004, National Common Minimum Programme of the Government of India,Government of India, New Delhi.

———2005a, Draft – National Pharmaceuticals Policy: 2006, Department of Chem-icals and Petrochemicals, Ministry of Chemicals and Fertilizers viewed 12February 2006, http://chemicals.nic.in/npp_circulation_latest.pdf.

———2005b, National Health Accounts 2001–02, National Health Accounts Cell,Ministry of Health and Family Welfare, New Delhi.

———2005c, The Patents (Amendment) Act, 2005, no. 15 of 2005, 5 April2005, viewed 16 November 2005, http://patentoffice.nic.in/ipr/patent/patent_2005.pdf.

———2005d, Pharmaceuticals, Department of Chemicals and Petrochemicals,viewed 12 December 2005, http://chemicals.nic.in/pharma1.htm.

———2005e, Report of the National Commission on Macroeconomics and Health,National Commission on Macroeconomics and Health, Ministry of Health andFamily Welfare, New Delhi.

———2005f, Seventh Report on Availability and Price Management of Drugs andPharmaceuticals, Standing Committee on Chemicals and Fertilizers (2005–06),Department of Chemicals and Petrochemicals, Ministry of Chemicals andFertilizers, New Delhi.

———2006a, Annual Report 2005–2006, Department of Chemicals andPetrochemicals, Ministry of Chemicals and Fertilizers, New Delhi.

———2006b, Census of India 2001: Population Projections for India and States2001–2026, Technical Group on Population Projections, Office of the RegistrarGeneral, New Delhi.

———2006c, (Draft) Towards Faster and More Inclusive Growth: An Approach to the11th Five-Year Plan, Planning Commission, New Delhi.

———2006d, Household Assets Holding, Indebtedness, Current Borrowings and Repay-ments of Social Groups in India: All-India Debt and Investment Survey, NSS 59thRound, no. 503 (59/18.2/4), National Sample Survey Organisation, Ministry ofStatistics & Programme Implementation, New Delhi.

———2006e, Morbidity, Health Care and the Condition of the Aged, NSS 60th Round,507 (60/25.0/1), National Sample Survey Organisation, Ministry of Statisticsand Programme Implementation, New Delhi.

———2006f, National Health Profile 2006, Central Bureau of Health Intelligence,Directorate General of Health Services, Ministry of Health and Family Welfare,New Delhi.

———2006g, ‘Notice for termination of exclusive marketing right EMR/1/2002’,The Patent Office Journal, no. 7, 17 February.

———2006h, Reduction in Prices of Certain Categories of Medicines (Promised),Department of Chemicals and Petro-Chemicals, Ministry of Chemicals andFertilizers, New Delhi, viewed 23 September 2008, http://chemicals.nic.in/ReductionList112006.pdf.

———2006i, Sectors Attracting Highest FDI Inflows, Department of Industrial Policyand Promotion, Ministry of Commerce & Industry, Government of India, NewDelhi.

———2006j, Selected Socio-economic Statistics India, Central Statistical Organisa-tion, Ministry of Statistics and Programme, New Delhi.

References 299

———2007a, ‘Actual reduction in prices of medicines as on 14 May 2007’, Depart-ment of Chemicals and Petrochemicals, Ministry of Chemicals and Fertilizers,New Delhi.

———2007b, Drugs and Pharmaceutical Exports (Commodity-wise), DirectorateGeneral Commercial Intelligence and Statistics (DGCIS), Kolkata.

———2007c, National Family Health Survey 2005–06 (NFHS-3), Ministry of Healthand Family Welfare, New Delhi.

———2007d, Report of the Special Subject Group: Unshackling Indian Industry, PrimeMinister’s Council on Trade and Industry, New Delhi.

———2007e, Report of the Working Group on Drugs and Pharmaceuticals for the 11thFive-Year Plan (2007–2012), Planning Commission of India, New Delhi.

———2007f, Statistical Pocket Book India, Combined Issue 2006 & 2007, 45thedn, Central Statistical Organisation, Ministry of Statistics and ProgrammeImplementation, New Delhi.

———2008a, Annual Report, Department of Scientific & Industrial Research,Ministry of Science and Technology, New Delhi.

———2008b, ‘Mainstreaming of ISM&H practitioners and bare-foot doctors’,viewed 23 June 2008, http://populationcommission.nic.in/ISM&H.htm.

———2009, ‘Annual Report’, Department of Pharmaceuticals, Ministry of Chem-icals and Fertilizers, New Delhi.

———2010, ‘List of Drugs Approved for Marketing in India’, Central Drugs Stan-dard Control Organisation, Directorate General of Health Services, Ministry ofHealth and Family Welfare, New Delhi.

Government of the United States 2008, The Orphan Drug Act (as Amended),SEC. 526 [360bb](a)(2), U.S. Food and Drug Administration, Washington, DC,viewed 24 August 2008, http://www.fda.gov/orphan/oda.htm.

Grabowski, H 2002, ‘Patents, innovation and access to new pharmaceuticals’,Journal of International Economic Law, vol. 5, no. 4, pp. 849–60.

———2005, ‘Increasing R&D incentives for neglected diseases: Lessons from theOrphan Drug Act’, in KE Maskus & JH Reichman (eds), International PublicGoods and Transfer of Technology under a Globalized Intellectual Property Regime,Cambridge University Press, New York, pp. 457–80.

Graf von der Schulenburg, JM 2007, Valuing Pharmaceutical Innovation inthe European Union: The German Perspective, Leibniz University, Hannover,Germany, Presentation, viewed 7 May 2008, http://www.lse.ac.uk/collections/LSEHealth/eventsAndSeminars/MerckSeminar2007/Workshopagendasandpresentations/ByMatthiasGrafvonderSchulenburg.pdf.

Gray, A & Matsebula, T 2003, ‘Drug pricing in South Africa- policy andpraxis’, Journal of Pharmaceutical Finance, Economics & Policy, vol. 12, no. 2,pp. 95–121.

Gupta, AS 2004, ‘Misplaced initiatives in the health sector’, People’s Democracy,vol. 28, no. 52.

Gupta, I & Trivedi, M 2005, ‘Social health insurance redefined: Health for allthrough coverage for all’, Economic and Political Weekly, vol. 40, no. 38,pp. 4132–40.

Hansen, R 1979, ‘The pharmaceutical development process: Estimates of devel-opment costs and times and the effects of proposed regulatory changes’, in RIChien (ed.), Issues in Pharmaceutical Economics, Lexington Books, D C Heath &Co, Lexington, MA.

300 References

Harten, C & Ballantyne, P 2004, ‘The impact of cost sharing within Canadianprovincial drug benefit programs: A review’, Journal of Pharmaceutical Finance,Economics & Policy, vol. 13, no. 1, pp. 35–53.

Harvey, K, Faunce, TA, Lokuge, B & Drahos, P 2004, ‘Will the Australia–UnitedStates Free Trade Agreement undermine the Pharmaceutical Benefits Scheme?’,The Medical Journal of Australia, vol. 181, no. 5, pp. 256–9.

Harvey, KJ 2005, ‘The Pharmaceutical Benefits Scheme 2003–2004’, Australia andNew Zealand Health Policy, vol. 2, no. 2.

Haub, C & Sharma, OP 2006, ‘India’s population reality: Reconciling change andtradition’, Population Bulletin, vol. 61, no. 3.

Hawthorne, F 2003, The Merck Druggernaut: The Inside Story of a PharmaceuticalGiant, John Wiley & Sons, Hoboken, New Jersey.

Hayek, FA 1988, The Fatal Conceit, University of Chicago Press, Chicago.Heinen, C & Perry, R 2006, ‘Big pharma’s Indian renaissance’, Scrip Magazine,

February, p. 33.Henry, D, Lopert, R & Lang, D 2001, Levelling the Playing Field: Using Evidence

to Determine ‘Fair’ Drug Prices, Paper presented to WHO/WTO Workshop onDifferential Pricing and Financing of Essential Drugs, Hosbjor, Norway, 8–11April, viewed 7 September 2005, http://www.wto.org/english/tratop_e/trips_e/hosbjor_presentations_e/37henry_e.pdf.

Hertz, AZ 1997, ‘Shaping the trident: Intellectual property under NAFTA, invest-ment protection agreements and at the World Trade Organization’, Canada-United States Law Journal, vol. 23, pp. 261–326.

Hesse, C 2002, ‘The rise of intellectual property, 700 B.C.–A.D. 2000: An idea inthe balance’, Daedalus, vol. 131, no. 2, pp. 26–45.

Hiddleston, S 2007, ‘No need to patent small changes’, Frontline, vol. 24, no. 5.Hoekman, B 2002, ‘The WTO: Functions and basic principles’, in B Hoekman,

A Mattoo & P English (eds), Development, Trade, and the WTO: A Handbook,The International Bank for Reconstruction and Development/The World Bank,Washington, DC.

Hofstede, G 2001, Culture’s Consequences: Comparing Values, Behaviors, Institutionsand Organizations Across Nations, Sage Publications, Thousand Oaks, Calif.

Hollis, A 2005, An Efficient Reward System for Pharmaceutical Innovation, Institute ofHealth Economics, Department of Economics, University of Calgary, Calgary.

Hope, J 2003, ‘Biotechnology project’, Open source, Research School of SocialSciences, Australian National University, Canberra, viewed 17 November 2006,http://rsss.anu.edu.au/∼janeth/Law.html.

House of Commons Health Committee 2005, The Influence of the PharmaceuticalIndustry, Government of the United Kingdom, London.

Hughes, JW, Moore, MJ & Snyder, EA 2002, ‘ “Napsterizing” pharmaceuticals:Access, innovation and consumer welfare’, Working paper no. 9229, NationalBureau of Economic Research, Cambridge, MA, October.

Humer, FB 2005, ‘Innovation in the pharmaceutical industry: Future prospects’,Talk to the Zuericher Volkswirtschaftliche Gesellschaft, Roche Pharmaceuticals,Zurich, 16 March.

Ibrahim, MIM & Bahri, S 2003, ‘Drug policies and pricing mechanism: TheMalaysian perspective’, Journal of Pharmaceutical Finance, Economics & Policy,vol. 12, no. 1, pp. 77–94.

References 301

IDR 2008, IDR Pharmacy Triple Compendium, Indian Drug Review, vol. 13,November 2007–January 2008.

IFPMA 2004, ‘Encouragement of New Clinical Drug Development: The Role ofData Exclusivity’, International Federation of Pharmaceutical ManufacturersAssociations, Geneva.

IMF 2008, ‘Report for selected countries and subjects’, World Economic OutlookDatabase, International Monetary Fund, Washington, DC, viewed 15 July 2008,http://www.imf.org/external/pubs/ft/weo/2008/01/weodata/weorept.aspx?sy=2006&ey=2013&scsm=1&ssd=1&sort=country&ds=.&br=1&c=534&s=NGDP_R%2CNGDP_RPCH%2CNGDP%2CNGDPD%2CNGDPPC%2CNGDPDPC%2CPPPGDP%2CPPPPC&grp=0&a=&pr.x=67&pr.y=2.

IMS Health 2004, IMS Lifecycle Incorporating R&D Focus, New Product Focus, andPatent Focus, CD, London, November.

INHATA 2008, ‘IQWiG – Institut für Qualität und Wirtschaftlichkeit imGesundheitswesen’, Global Networking for Effective Healthcare, viewed 30September 2008, http://www.inahta.org/Members/IQWiG/.

Insurance Regulatory and Development Authority (IRDA) 2007, Annual Report2005–06, Hyderabad.

———2008, Annual Report 2006–07, Hyderabad.Inter-Ministerial Consultative Committee (IMCC) 2007, Report on Steps to be Taken

by Government of India in the Context of Data Protection Provisions of Article 39.3of TRIPS Agreement, Department of Chemicals and Petrochemicals, Ministry ofChemicals and Fertilizers, Government of India, New Delhi.

IP-Watch 2006, ‘Pretest submitted to first patent filing of HIV/AIDS drug in India’,Intellectual Property Watch, Geneva, viewed 28 October 2008, http://www.ip-watch.org/weblog/index.php?p=254&print=1.

Jack, W & Lanjouw, JO 2005, ‘Financing pharmaceutical innovation: How muchshould poor countries contribute?’, The World Bank Economic Review, vol. 19,no. 1, January, pp. 45–67.

Jatania, P 2004, ‘In search of the sugar-coating: The new product patents regimewill decide the future of hundreds of leukaemia patients’, Indian Express, 19December.

Jeremy, D 2004, ‘Patents and Technology Transfer Between Nations: 1790–1851:Help, Hindrance or Irrelevance: Lessons from History’, paper presented to Intel-lectual Property Rights, Economic Development, and Social Welfare: What doesHistory tell us?, Ironbridge Gorge Museum, Coalbrookdale, 26 April.

Jorge, MF 2004, ‘TRIPS-plus provisions in trade agreements and their potentialadverse effects on public health’, Journal of Generic Medicines, vol. 1, no. 3,pp. 199–211.

Jyothi-Datta, PT 2006, ‘Roche gets product patent on Hepatitis C’, The HinduBusiness Line, 3 March.

Kamath, G 2004, ‘Is the pharma dream run over?’, Business World India,1 November.

———2007, ‘Beyond generics: Indian pharma companies are hiving off R&Dunits into separate companies in their quest for new drugs’, Business World,28 December.

Kamath, G & Krishnan, GS 2004, ‘Generics market: Creeping acquisition’,Business World, 2 August, p. 8.

302 References

Kassirer, JP 2005, On the Take: How Medicine’s Complicity with Big Business canEndanger your Health, Oxford University Press, New York.

Kaul, S 2004, ‘In better health than ever: Zydus Cadila prepares itself forthe challenges of the post WTO era’, Business India, 26 April–9 May,pp. 61–5.

Keayla, BK 1996, ‘New patent regime: Implications for domestic industry,research and development and consumers’, National Working Group on PatentLaws, Centre for Study on GATT Laws, New Delhi.

Khan, BZ 2002, ‘Intellectual property and economic development: Lessons fromAmerican and European history’, Study paper 1a, Commission on Intellec-tual Property Rights, viewed 24 October 2008, http:www.iprcommission.org/papers/word/study_papers/sp1a_khan_study.doc.

Khosla, R & Hunt, P 2008, Human Rights Guidelines for Pharmaceutical Compa-nies in Relation to Access to Medicines, Human Rights Centre, University ofEssex, viewed 1 February 2010, http://www.essex.ac.uk/human_rights_centre/research/rth/docs/Final_pharma_for_website.pdf.

Klein, N 2003, ‘Bush’s AIDS test’, The Nation, 27 October, p. 12.Knowledge at Wharton 2008, ‘An increasingly affluent Middle India is harder

to ignore’, India Knowledge@Wharton, viewed 12 July 2008, http://knowledge.wharton.upenn.edu/india/articlepdf/4303.pdf?CFID=74092837&CFTOKEN=85340977&jsessionid=9a3095fb819e56262155.

Koshy, S 1995, ‘The effects of TRIPS on Indian Patent Law: A pharmaceuticalperspective’, Boston University Journal of Science & Technology Law, vol. 1, no. 4,pp. 123–49.

KPMG 2006a, The Indian Pharmaceutical Industry: Collaboration for Growth, KPMGInternational, Mumbai.

KPMG 2006b, India Pharma Inc Competing Globally, KPMG International, Mumbai.Kremer, M 2002, ‘Pharmaceuticals and the developing world’, Journal of Economic

Perspectives, vol. 16, no. 4, pp. 67–90.Kremer, M & Glennerster, R 2004, Strong Medicine: Creating Incentives for Pharma-

ceutical Research on Neglected Diseases, Princeton University Press, Princeton.Kumar, R 2008, ‘Encourage innovation with holistic approach: Basheer’, The

Hindu Business Online, 13 October, viewed 31 October 2008, http://www.hindu.com/biz/2008/10/13/stories/2008101350051600.htm.

Labonte, R & Schrecker, T 2006, Globalization and Social Determinants of Health:Analytic and Strategic Review Paper, Institute of Population Health, Universityof Ottawa, 11 March, viewed 11 November 2008, http://www.who.int/social_determinants/resources/globalization.pdf.

Lacetera, N 2001, ‘Corporate governance and the governance of innovation: Thecase of the pharmaceutical industry’, Journal of Management and Governance,vol. 5, no. 1, pp. 29–59.

Lalitha, N 2002, ‘Indian pharmaceutical industry in WTO regime’, Economic andPolitical Weekly, vol. 37, no. 34, 24–30 August.

Lall, S 1974, ‘The international pharmaceutical industry and less-developed coun-tries, with special reference to India’, Oxford Bulletin of Economics and Statistics,vol. 36, no. 3, pp. 143–72.

Lanjouw, J 1998, ‘The Introduction of pharmaceutical product patents in India:Heartless exploitation of the poor and suffering?’, Working paper no. 6366,National Bureau of Economic Research, Cambridge, MA, January.

References 303

———2002a, ‘A new global patents regime for diseases: U.S, and interna-tional legal issues’, Harvard Journal of Law & Technology, vol. 16, no. 1, Fall,pp. 1–40.

———2002b, ‘Intellectual property and the availability of pharmaceuticals inpoor countries’, CGD Working paper no. 5, Centre for Global Development,April, viewed 24 May 2004, http://www.cgdev.org/content/publications/detail/2785.

Lanjouw, JO & Cockburn, IM 2001, ‘New pills for poor people? Empiricalevidence after GATT’, World Development, vol. 29, no. 2, pp. 265–89.

Lehman, B 2003, The Pharmaceutical Industry and the Patent System, Earth Insti-tute, Columbia University, viewed 12 June 2007, http://www.earthinstitute.columbia.edu/cgsd/documents/lehman.pdf.

Lewis, G, Class, S & Edery, E 2005, ‘Growth in moderation’, Scrip Magazine,February, pp. 28–33.

Lichtenberg, FR 2006, ‘Importation and innovation’, Working paper no. 12539,National Bureau of Economic Research, Cambridge, MA, September.

Light, DW 2005, ‘Making practical markets for vaccines’, PLoS Medicine, vol. 2,no. 10, p. 271.

Lippoldt, D 2006, ‘Intellectual property rights, pharmaceuticals and foreigndirect investment’, Policy brief, Groupe d’Economie Mondiale de SciencesPo., Paris, November, viewed 27 April 2008, http://gem.sciences-po.fr/content/publications/pdf/lippoldt_IPRs_Pharma_FDI1106.pdf.

Lleras-Muney, A & Lichtenberg, FR 2002, ‘The effect of education on medicaltechnology adoption: Are the more educated more likely to use new drugs?’,Working paper, no. 9185, National Bureau of Economic Research, Cambridge,MA, September.

Lloyd, I 2002, ‘R&D revolution remains just around the corner’, Scrip Magazine,February, pp. 72–3.

Lofgren, H 2005, ‘Purchase commitments: Big business bias or solution to the‘Neglected Disease’ dilemma?’, Australian Review of Public Affairs, 31 October,viewed 12 December 2005, http://www.australianreview.net/digest/2005/10/lofgren.html.

———2007, ‘Reshaping Australian drug policy: The dilemmas of genericmedicines policy’, Australia and New Zealand Health Policy, vol. 4, no. 11,pp. 1–4.

Macdonald, S 2002, ‘Exploring the hidden costs of patents’, in P Drahos &R Mayne (eds), Global Intellectual Property Rights: Knowledge, Access and Devel-opment, Palgrave Macmillan, New York, pp. 13–39.

Machlup, F 1958, An Economic Review of the Patent System: Study of the Subcom-mittee on Patents, Trademarks, and Copyrights of the Committee on the Judiciary,Presented to Eighty Fifth Congress, Study no. 15, United States Senate,Government of the United States, Washington, DC.

Machlup, F & Penrose, E 1950, ‘The patent controversy in the nineteenthcentury’, The Journal of Economic History, vol. 10, no. 1, pp. 1–29.

Madanmohan, TR & Krishnan, RT 2003, ‘Adaptive strategies in the Indianpharmaceutical industry’, International Journal of Technology and Management,vol. 25, no. 3–4, pp. 227–46.

Mahal, A 2000, ‘Private entry into health insurance in India: An assessment’,in D Peters, GNV Ramana & KS Rao (eds), Private Health Insurance and Public

304 References

Health Goals in India, Report on a National Seminar, World Bank, New Delhi,pp. 46–76.

———2002, ‘Health policy challenges for India: Private health insurance andlessons from the international experience’, in TN Srinivasan (ed.), Trade,Finance and Investment in South Asia, Social Science, New Delhi, pp. 395–463.

Malhotra, P 2008, ‘The impact of TRIPS on innovation and exports: A case studyof the pharmaceutical industry in India’, Indian Journal of Medical Ethics, vol. 5,no. 2, pp. 61–5.

Malhotra, P & Grewal, B 2008, ‘TRIPS-plus: Free trade agreements jeopardisingpublic health in developing nations’, in TV Hoa & C Harvie (eds), RegionalTrade Agreements in Asia, Edward Elgar, Cheltenham, UK, pp. 216–39.

Managing Intellectual Property 2007, ‘AIDS patent first in India’, Weekly News, 19December.

Mansfield, E 1986, ‘Patents and innovation: An empirical study’, ManagementScience, vol. 32, no. 2, pp. 173–81.

———1995, ‘Intellectual property protection, direct investment, technologytransfer: Germany, Japan and the United States’, Discussion paper no.27, International Finance Corporation, The World Bank, Washington, DC,September.

Mashelkar, RA 2003, ‘Whither India with the international patents regime?’,Chemical Business, April–June, pp. 77–92.

Maskus, K 2000a, ‘Intellectual Property Rights and Foreign Direct Investment’,Centre for International Economic Studies, University of Adelaide, Adelaide,Australia, May.

———2000b, ‘Regulatory standards in the WTO’, Working paper 00-1, Institutefor International Economics, Washington, January, viewed 16 November 2004,http://www.iie.com/publications/wp/wp.cfm?ResearchID=121.

Maskus, KE & Reichman, JH 2004, ‘The globalization of private knowledge goodsand the privatization of global public goods’, Journal of International EconomicLaw, vol. 7, no. 2, pp. 279–320.

Mathew, J 2006, ‘Ranbaxy eyes stake in marketing allies’, Economics Times, 12July, viewed 19 July 2006, http://economictimes.indiatimes.com/articleshow/1733416.cms.

———2008, ‘Cipla unveils Roche’s generic version of anti-infection drug’, Busi-ness Standard, 24 September.

Mathew, T & Torreblanca, M 2005, ‘India steps up to the plate’, Scrip Magazine,November, pp. 47–9.

Mathieu, MP (ed.) 2007, Parexel’s Bio/Pharmaceutical R&D Statistical Sourcebook2007/2008, Parexel International Coroporation, Waltham, MA, USA.

May, C & Sell, S 2006, Intellectual Property Rights: A Critical History, Lynne Rienner,Boulder, Colorado.

Mayne, R 2002, ‘The global campaign on patents and access to medicines: AnOxfam perspective’, in P Drahos & R Mayne (eds), Global Intellectual Prop-erty Rights: Knowledge, Access and Development, Palgrave Macmillan, New York,pp. 244–58.

———2005, ‘Regionalism, bilateralism, and ‘TRIPS Plus’ agreements: The threatto developing countries’, United Nations Development Program, OccasionalPaper no. 2005/18, viewed 6 September 2005, http://hdr.undp.org/docs/publications/background_papers/2005/HDR2005_Mayne_Ruth_18.pdf.

References 305

Mazumdar-Shaw, K 2007, ‘Biotechnology Partnering Opportunities with India’,paper presented to BioBreakfast, Melbourne Town Hall, 16 March.

McEwan, JG 2005, ‘Is the cure worse than the disease? An overview of the PatentReform Act of 2005’, The John Marshall Review of Intellectual Property Law, vol. 5,no. 1, pp. 55–77.

McLachlan, AJ, Ramzan, I & Milne, RW 2007, ‘Frequently asked questions aboutgeneric medicines’, Australian Prescriber, vol. 30, no. 2, pp. 41–3.

Medicines Australia 2008, ‘Global pharmaceutical industry: Facts at a glance’,Canberra, March, viewed 17 November 2008, http://www.medicinesaustralia.com.au/pages/images/Global%20-%20facts%20at%20a%20glance.pdf.

Medico Friends Circle 2006, ‘Submission to the Government of India: A balancedpharmaceutical policy’, Pune, 10 July, viewed 17 October 2008, http://www.mfcindia.org/PMdrugpricing.html.

MedIndia 2007, ‘Patents: Appellate board becomes functional’, MedIndia.com,Chennai, 10 April, viewed 28 May 2007, http://www.medindia.net/news/view_news_main.asp?x=19886.

Melethil, S 2005, ‘Patent issues in drug development: Perspectives of a pharma-ceutical scientist-attorney’, The American Association of Pharmaceutical Scientists(AAPS) Journal, vol. 7, no. 3, pp. E723–28.

Minwalla, S 2003, ‘Drug promotion in India’, Healthy Skepticism InternationalNews, vol. 21, no. 9, viewed 10 June 2008, http://www.healthyskepticism.org/publications/editions/2003/9.htm.

Misra, R, Chatterjee, R & Rao, S 2003, India Health Report, Oxford University Press,New Delhi.

Mokyr, J 1990, The Lever of Riches: Technological Creativity and Economic Progress,Oxford University Press, London.

Morag-Sela, T, Cohn, I, Kowalski, TJ, Jarecki-Black, J & Clyde-Watson, Z 2004,‘Intellectual property law in Israel, and US and European objections: Mar-ket exclusivity vs. data exclusivity’, Nature Biotechnology, vol. 22, no. 12,pp. 1591–2.

Moran, M 2001, ‘Bitter medicine: Why the developing world can’t get drugs’,On Line Opinion, 15 April, viewed 25 January 2006 http://www.onlineopinion.com.au/view.asp?article=1971.

———2005, ‘A breakthrough in R&D for neglected diseases: New ways toget the drugs we need’, PLOS, vol. 2, no. 9, viewed 12 December2005, http://medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0020302.

MSF 2008, ‘Pre-grant opposition victory in India’, Campaign for Access to Essen-tial Medicines, viewed 28 October 2008, http://www.msfaccess.org/main/access-patents/pre-grant-opposition-victory-in-india/.

Mueller, JM 2007a, ‘Taking TRIPS to India: Novartis, patent law, access tomedicines’, The New England Journal of Medicine, vol. 356, no. 6, pp. 541–3.

———2007b, ‘The tiger awakens: The tumultuous transformation of India’spatent system and the rise of Indian pharmaceutical innovation’, University ofPittsburgh Law Review, vol. 68, no. 3, pp. 491–641, viewed 24 April 2007, http://lawreview.law.pitt.edu/issues/68/68.3/Mueller.pdf.

Mukherjee, S 2005, ‘Pharmaceutical research and development in India – Lookingup?’, Business Briefing: Pharma Outsourcing, 11 March, pp. 98–103.

Mukreja, DN 2004, ‘Against all sceptics’, Business World, 16 August, pp. 29–34.

306 References

Murray, CJL & Lopez, AD (eds) 1996, The Global Burden of Disease: A Compre-hensive Assessment of Mortality and Disability from Diseases, Injuries, and RiskFactors in 1990 and Projected to 2020, Global Burden of Disease and Injury Series,Volume I, The Harvard School of Public Health on behalf of the World HealthOrganization and the World Bank, Cambridge, MA.

mX 2006, ‘Record deal ends tax row’, mX, 12 September, p. 11.Nagendranath, A & Chari, P 2002, Health Insurance in India: The Emerging

Paradigms, Paper presented to Insurance ’02: A Seminar on the EmergingIssues in the Indian Insurance Sector, IIFT-School of International BusinessManagement, New Delhi, 6 September.

Nanda, N 2006, Options for Using Competition Law/Policy Tools in Dealing withAnti-Competitive Practices in the Pharmaceutical Industry and the Heath DeliverySystem, Report Prepared for World Health Organization & Ministry of Healthand Family Welfare, Government of India, CUTS Centre for Competition,Investment and Economic Regulation (CUTS C-CIER), CUTS International,Jaipur.

Nanda, N & Khan, A 2005, ‘Competition policy for the pharmaceuticals sectorin India’, in P Mehta (ed.), Towards a Functional Competition Policy for India,Academic Foundation, New Delhi.

Nard, CA & Morriss, AP 2006, ‘Constitutionalizing patents: From Venice toPhiladelphia’, Review of Law & Economics, vol. 2, no. 2, pp. 223–321.

Narrain, S 2004, ‘A life-saving order’, Frontline, vol. 21, no. 15.———2005, ‘A costly prescription’, Frontline, vol. 22, no. 4.Narula, R 2004, ‘A recipe for litigation’, Scrip Magazine, June, p. 39.NIPER 2006, Impact of TRIPS on Pharmaceutical Prices, with Specific Focus on Generics

in India, National Institute of Pharmaceutical Education and Research, Depart-ment of Chemicals and Petrochemicals, Ministry of Chemicals and Fertilizers,Government of India, Mohali.

NISTADS 2005, Indian Patenting Activity in International and Domestic Patent System:Contemporary Scenario, National Institute of Science Technology and Develop-ment Studies, Office of the Principal Scientific Advisor to the Government ofIndia, New Delhi.

Nordmann, RM 1997, ‘A quarter century of monumental change’, Scrip Magazine,April, pp. 28–9.

North, DC 1968, ‘Source of productivity change in ocean shipping 1600–1850’,Journal of Political Economy, vol. 76, no. 5, September/October, pp. 953–70.

Novartis 2004, ‘Novartis India Analyst Meeting’, Novartis India, 16 July 2004.Nunnenkamp, P & Spatz, J 2003, ‘Intellectual property rights and foreign direct

investment: The role of industry and host-country characteristics’, Kiel Work-ing Paper no. 1167, Kiel Institute for World Economics, Kiel, Germany,June.

OECD 2001, Report on Competition and Regulation Issues in the Pharmaceu-tical Industry, Organisation for Economic Co-operation and Development,Paris.

———2008, Pharmaceutical Pricing Policies in a Global Market, Directoratefor Employment, Labour and Social Affairs, Organisation for EconomicCo-operation and Development, Paris.

OneIndia 2007, ‘Rs 750 Crore Rashtriya Swasthya Bima Yojana Launched’, viewed17 June 2008, http://news.oneindia.mobi/2007/10/03/451757.html.

References 307

OPPI 2003, ‘Pharmaceutical Industry in India: Fact Sheet – 2003’, Organisationof Pharmaceutical Producers of India, Mumbai, viewed 9 August 2005. http://www.indiaoppi.com/keystat.htm.

———2006, ‘Indian pharmaceutical industry: Fact sheet – 2004’, Organisationof Pharmaceutical Producers of India, viewed 12 February 2006, http://www.indiaoppi.com/keystat.htm.

Outterson, K 2008, ‘Should access to medicines and TRIPS flexibilities be lim-ited to specific diseases?’, American Journal of Law & Medicine, vol. 34, no. 2,pp. 317–38.

Oxfam 2002, Rigged Rules and Double Standards: Trade, Globalisation, and the FightAgainst Poverty, Oxfam International, London.

Palit, A & Nawani, S 2007, ‘Technological capability as a determinant of FDIinflows: Evidence from developing Asia and India’ Working paper no. 193,Indian Council for Research on International Economic Relations, New Delhi,April, viewed 23 September 2008, http://www.icrier.org/pdf/Working_Paper_193.pdf.

Pammolli, F & Riccaboni, M 2007, Innovation and Industrial Leadership: Lessonsfrom Pharmaceuticals, Center for Transatlantic Relations, The Johns HopkinsUniversity, Washington, DC.

Patent Lens 2009, ‘Initiative for open innovation’, Canberra, viewed 9 January2009, http://www.patentlens.net/daisy/patentlens/2973.html.

Patnaik, U 2010, ‘Trends in Urban Poverty Under Economic Reforms: 1993–94 to2004–05’, Economic and Political Weekly, vol. 45, no. 4, pp. 42–54.

Perlitz, U 2008, India’s Pharmaceutical Industry on Course for Globalisation,Deutsche Bank Research, Frankfurt, 9 April, viewed 11 August 2008, http://www.dbresearch.com/PROD/DBR_INTERNET_EN-PROD/PROD0000000000224095.pdf.

Pettypiece, S 2006, ‘Pfizer shops for drugs, profits’, Detroit Free Press, 1July, viewed 3 July 2006, http://www.freep.com/apps/pbcs.dll/article?AID=20060701/BUSIENESS06/607010363/1019/BUSINESS.

Pfizer 2005, Hatch-Waxman Economics: Balanced Incentives are the Key, Pfizer Inc,New York.

———2007, Annual Review, Pfizer Inc. New York.Phadke, A 2000, ‘End of drug control?’, India-Seminar, viewed 25 September 2008,

http://www.india-seminar.com/2000/489/489%20phadke.htm.Pharmaceutical & Drug Manufacturers 2005a, ‘Indian pharmaceutical indus-

try: An overview’, viewed 12 June 2005, http://www.pharmaceutical-drug-manufacturers.com/pharmaceutical-industry/.

———2005b, ‘Number of units, pharma industry statistics’, viewed 3 November2005, http://www.pharmaceutical-drug-manufacturers.com/pharma-industry-statistics/.

PhRMA 2002, Annual Report, Pharmaceutical Research and Manufacturers ofAmerica, Washington, DC.

———2004, Industry Profile, Pharmaceutical Research and Manufacturers ofAmerica, Washington.

———2007, Annual Report, Pharmaceutical Research and Manufacturers ofAmerica, Washington, DC.

———2008a, Annual Report, Pharmaceutical Research and Manufacturers ofAmerica, Washington, DC.

308 References

———2008b, Pharmaceutical Industry Profile 2008, Pharmaceutical Research andManufacturers of America, Washington, DC.

Pogge, T 2008, ‘Access to medicines’, Public Health Ethics, vol. 1, no. 2, pp. 73–82.Posner, RA 2002, ‘The law and economics of intellectual property’, Daedalus,

vol. 131, no. 2, pp. 5–12.Pradhan, S 1983, International Pharmaceutical Marketing, Quorum Books,

Westport, CT.Prahalad, CK 2005, The Fortune at the Bottom of the Pyramid: Eradicating Poverty

Through Profits, Wharton School Publishing, Upper Saddle River, NJ.Public Citizen 2001, Rx R&D myths: The Case Against the Drug Industry’s Scare Card,

Public Citizen Congress Watch, Washington, DC, July, viewed 9 September2003, http://www.citizen.org/documents/ACFDC.PDF.

Pugatch, MP 2004, Intellectual Property and Pharmaceutical Data Exclusivity in theContext of Innovation and Market Access, paper presented to Dialogue on Ensur-ing Policy Options for Affordable Access to Essential Medicines, Bellagio, Italy,12–16 October.

Ram, P 2006, ‘India’s new TRIPS-Compliant patent regime: Between drug patentsand the right to health’, Chicago-Kent Journal of Intellectual Property, vol. 5, no. 2,Spring, pp. 195–206.

Rangnekar, D 2005, ‘No pills for poor people? Understanding the disembowel-ment of India’s patent regime’, Economic and Political Weekly, vol. 41, no. 5,pp. 409–17.

Raymus, P 2007, Review of Healthcare in India, Centre for Enquiry into Health andAllied Themes, New Delhi, January, viewed 1 July 2008, http://www.cehat.org/infocentre/r51tables1.pdf#page=373.

Reichman, JH 2000, ‘The TRIPS Agreement comes of age: Conflict of cooperationwith the developing countries?’, Case Western Reserve Journal of InternationalLaw, vol. 32, no. 3, pp. 441–70.

Reichmann, JH 1998, ‘Securing compliance with the TRIPS agreement after US vIndia’, Journal of International Economic Law, vol. 1, no. 4, pp. 586–601.

Reserve Bank of India (RBI) 2005, Exchange Control Manual: Foreign/FERA Com-panies and Foreign Nationals, Reserve Bank of India, Government of India,31 May, viewed 21 February 2007, http://www.rbi.org.in/upload/ECM/pdfs/Chapter11.pdf.

———2007, State Finances: A Study of Budgets of 2006–07, Reserve Bank of India,Government of India, New Delhi.

———2008, Annual Report 2007–08, Reserve Bank of India, Government of India,New Delhi.

Rhein, R 2001, ‘Canada keeps costs in check’, Scrip Magazine, February, pp. 24–5.Rogers, A 1994, ‘Patents in Argentina: Problems and paradoxes’, Scrip Magazine,

December, pp. 10–1.Roumeliotis, G 2006, ‘India set to overtake Italy in API production’, viewed 28

August 2006, http://www.in-pharmatechnologist.com/Materials-Formulation/India-set-to-overtake-Italy-in-API-production.

Roy, N & Madhiwala, N 2003, Surviving the Indian Pharmatical Jungle, Forum forMedical Ethics, Mumbai.

Ruston, G 1955, ‘On the origin of trademarks’, The Trade-Mark Reporter, vol. 45,no. 2, pp. 127–44.

Sachs, JD 2000, ‘A new map of the world’, The Economist, 22 June.

References 309

Sager, A & Socolar, D 2006, ‘Massachusetts health spending soars to $62.1billion in 2006: Spending here is world’s highest – 33% per person aboveUSA average, an unprecedented excess’, Boston University School of PublicHealth, Health Reform Program, Boston, 28 June, viewed 17 July 2007, http://dccwww.bumc.bu.edu/hs/Mass%20Health%20Spending%20Soars%20to%20$62%201%20Billion%20in%202006%20FINAL%2028June.pdf.

Sakthivel, S 2005, ‘Access to essential drugs and medicine’, Financing and Deliveryof Health Care Services in India, Commission on Macroeconomic and Health,and Ministry of Health and Family Welfare, New Delhi, pp. 185–212.

Santerre, RE & Vernon, JA 2005, ‘Assessing consumer gains from a drug price con-trol policy in the U.S.’, Working paper no. 11139, National Bureau of EconomicResearch, Cambridge, MA, February.

———2006, ‘Assessing consumer gains from a drug price control policy in theUnited States’, Southern Economic Journal, vol. 73, no. 1, pp. 233–45.

Sauer, C & Sauer, RM 2007, ‘Is it possible to have cheaper drugs and preserve theincentive to innovate? The benefits of privatizing the drug approval process’,Journal of Technology Transfer, vol. 32, no. 5, pp. 509–24.

Saunders, P 1999, ‘It’s time to call a halt to poor drug donation practice’, ScripMagazine, September, pp. 7–9.

Scherer, FM 2000, ‘The pharmaceutical industry’, in JP Newhouse (ed.), Handbookof Health Economics, Volume. I, Elsevier, Amsterdam, pp. 1297–336.

———2001, ‘The link between gross profitability and pharmaceutical R&Dspending’, Health Affairs, vol. 20, no. 5, September/October, pp. 216–20.

———2002, ‘A Note on Global Welfare in Pharmaceutical Patenting’, FederalReserve Bank of Philadelphia, Philadelphia, November, Working paper no.03–11, viewed 11 May 2007, <http://ssrn.com/abstract=570565>.

———2007, ‘Uncertainty and choice: The challenges of pharmaceutical effi-cacy, safety and cost’, Managerial and Decision Economics, vol. 28, no. 4–5,pp. 267–83.

Scherer, FM & Watal, J 2001, The Economics of Parallel Trade in Pharma-ceutical Products, Paper presented to WHO/WTO Workshop on DifferentialPricing and Financing of Essential Drugs, Hosbjor, Norway, 8–11 April,viewed 5 January 2004, http://www.wto.org/english/tratop_e/trips_e/hosbjor_presentations_e/hosbjor_presentations_e.htm.

Scherer, FM & Weisburst, S 1995, ‘Economic effects of strengthening pharmaceu-tical patent protection in Italy’, International Review of Industrial Property andCopyright Law, vol. 138, no. 26, pp. 1009–24.

Schiff, E 1971, Industrialisation Without National Patents: The Netherlands,1869–1912; Switzerland, 1850–1907, Princeton University Press, Princeton, NJ.

Schneider, F & Frey, BS 1985, ‘Economic and political determinants of foreigndirect investment’, World Development, vol. 13, no. 2, pp. 161–75.

Schreyoegg, J & Busse, R 2005, ‘Physician-drug budgets in Germany and effects onprescription behaviour’, Journal of Pharmaceutical Finance, Economics & Policy,vol. 14, no. 3, pp. 77–95.

Schweitzer, SO 1997, Pharmaceutical Economics and Policy, Oxford UniversityPress, New York.

Scott, A 2006, ‘Blockbuster drug numbers increase’, Chemical Week, vol. 168,no. 12, p. 31.

Scrip 2006, ‘Company partnerships’, Scrip 100, Informa Plc, London, p. 25.

310 References

Scrip News 2005a, ‘Canadian industry can expel firms for marketing offences’,Scrip News, no. 3114, 9 December.

———2005b, Indian proposal for generic prescribing opposed, Scrip News,vol. 3072, 15 July, p. 18.

———2005c, ‘US payers stand to benefit from targeted medicine’, Scrip News,vol. 3117, p. 13.

———2005d, ‘World’s scientists get $436 million to tackle diseases’, Scrip News,vol. 3069, p. 15.

Sen, A 2002, ‘How to judge globalism: Global links have spread knowledgeand raised average living standards, but the present version of globalismneedlessly harms the world’s poorest’, The American Prospect, vol. 13, no. 1,pp. A2–6.

Seyoum, B 1996, ‘The impact of intellectual property rights on foreign directinvestment’, Columbia Journal of World Business, vol. 31, no. 1, pp. 50–9.

Shadlen, K 2009, ‘Reforming and reinforcing the revolution: The post-TRIPSpolitics of patents in Latin America’, Working paper no. 09–02, Globaldevelopment and Environment Institute, Tufts University, April.

Shah, D 2003, Experience of India, Paper presented to The Role of Genericsand Local Industry in Attaining the MDGs in Pharmaceuticals andVaccines, World Bank, Washington, DC, 24–25 June, viewed 4 July2007, wbln0018.worldbank.org/HDNet/hddocs.nsf/9b2b70eeb6c333fb852568aa0073e2a1/dc5eece4d602253685256d4a004c41ce.

Shiva, V 2004, ‘TRIPS, human rights and the public domain’, The Journal of WorldIntellectual Property, vol. 7, no. 5, pp. 665–73.

Singh, K 2008, ‘NGO to seek compulsory licensing of cancer drugs’, EconomicTimes, 31 March.

Singleton, A 2006, ‘Can pharmaceuticals be developed without patents?’,Samizdata.net, London, 9 January, viewed 23 February 2006, http://www.samizdata.net/blog/archives/008450.html.

Sketris, I, Bowles, S & Manuel, R 2003, ‘Canadian public policies and practicesrelated to drug prices, utilization and expenditures’, Journal of PharmaceuticalFinance, Economics & Policy, vol. 12, no. 1, pp. 23–54.

Smith, SE 2000, Opening Up to the World: India’s Pharmaceutical Companies Pre-pare for 2005, Asia/Pacific Research Center, Institute for International Studies,Stanford University, Stanford.

So, AD 2004, ‘A fair deal for the future: Flexibilities under TRIPS’, Bulletin of theWorld Health Organization, vol. 82, no. 11, pp. 813–4.

Solow, RM 1957, ‘Technical change and the aggregate production’, The Review ofEconomics and Statistics, vol. 39, no. 3, August, pp. 312–20.

Srinivasan, S 2008, ‘How TRIPS benefits Indian industry and how it may notbenefit the Indian people’, Indian Journal of Medical Ethics, vol. V, no. 2,pp. 66–9.

Stiglitz, JE 2002a, ‘Globalism’s discontents: Integration with the global econ-omy works just fine when sovereign countries define the terms, it worksdisastrously when terms are dictated’, The American Prospect, vol. 13, no. 1,pp. A16–21.

———2002b, Globalization and its Discontents, W.W. Norton & Company,New York.

———2006, Making Globalization Work, W.W. Norton and Company, New York.

References 311

Stoate, N 2001/2002, ‘EU enlargement, the Bolar exemption and parallel imports:The consequences for market exclusivity’, Bio Science Law Review, vol. 5, no. 5,pp. 161–82.

Swain, N, Mishra, C, Jayasimha, K & Vijayalakshmi, S 2002, ‘Indian pharmaceu-tical industry: An analysis’, The Icfaian Journal of Management Research, vol. 1,no. 6, pp. 5–28.

Sweeny, K 2002, The Technological Revolution, Paper presented to Pharmaceuticalsin Australia: Access, Costs and Industry Development, Melbourne, 16September.

———2008, ‘Accounting for growth in the pharmaceutical benefits scheme’, PhDBook, Victoria University, Melbourne, Australia, April.

Tamilnadu Pharmaceutical Sciences Welfare Trust 2008, ‘Drugs approved by theDrugs Controller General (India) during January 1988 to August 2006’, viewed12 December 2008, http://www.pictrust.com/links/newdrugs.phtml.

Taylor, P 2005, ‘Sun pharma buys hungarian plant’, In-Pharmatechnologist, viewed9 September 2005, http://www.in-pharmatechnologist.com/news/news-ng.asp?id=61850-sun-generic-india-hungary.

The Economist 2005a, ‘Alternative medicine: Neglected diseases are fighting forattention’, The Economist, 16 June, pp. 8–9.

———2005b, ‘Health at a glance: OECD indicators’, The Economist, 16 June.The Expert Committee 2003, Report of the Expert Committee on a Comprehensive

Examination of Drug Regulatory Issues, Including the Problem of Spurious Drugs,Ministry of Health and Family Welfare, Government of India, New Delhi.

The Sen Committee 2005, Report: Task Force to Explore Options Other Than PriceControl for Achieving the Objective of Making Available Life-Saving Drugs at Rea-sonable Prices, Department of Chemicals and Petrochemicals, Government ofIndia, New Delhi.

The Seth Committee 2004, National List of Essential Medicines 2003, DirectorateGeneral of Health Services, Ministry of Health and Family Welfare, Govern-ment of India, New Delhi.

The Tribune 2004, ‘Government to cut prices of drugs’, The Tribune, 22 December.The Wharton School 2008, Eli Lilly’s Rajiv Gulati on Pharma’s Prospects in

India and China, The Wharton School, The University of Pennsylvania, 16October, viewed 18 October 2008, http://knowledge.wharton.upenn.edu/india/articlepdf/4325.pdf?CFID=75279634&CFTOKEN=29111060&jsessionid=a83096d931ea33394241.

Timmermans, K 2007, ‘Monopolizing clinical trial data: Implications and trends’,PLoS Medicine, vol. 4, no. 2, pp. 206–10.

Torbet, J 1999, ‘Globalisation and its impact on access to medicines’, ScripMagazine, May, pp. 8–10.

UNCTAD 2005, World Investment Report: Transnational Corporations and the Inter-nationalization of R&D, United Nations Conference on Trade and Development,New York.

———2007, World Investment Report: Transnational Corporations, Extractive Indus-tries and Development, United Nations Conference on Trade and Development,New York.

UNCTC 1993, World Investment Report: Transnational Corporations and IntegratedInternational Production, The United Nations Centre on Transnational Corpora-tions, New York.

312 References

UNDP 2003, Making Global Trade Work for People, Earthscan Publications, London.———2005, Human Development Report, United Nations Development Pro-

gramme, Geneva.United Nations 2005a, India Demographic Profile 2000–2050, United Nations Pop-

ulation Division, Department of Economic and Social Affairs, New York, viewed12 August 2008, http://esa.un.org/unpp/p2k0data.asp.

———2005b, World Population Prospects: The 2004 Revision, Department of Eco-nomic and Social Affairs, Population Division, New York.

Verband der Forschender Arzeneimittelhersteller 2007, Heath Care Reform 2007,German Association of Research-based Pharmaceutical Companies, 27 March,viewed 23 July 2007, http://www.vfa.de/en/articles/art_2007-03_010.html.

Verheugen, G 2005, ‘Commission push on pharma innovation’, viewed1 June 2007, http://www.euractive.com/Article?tcmuri=tcm:29-140360-16&type=News.

Vernon, JA & Manning, RL 2007, ‘Editorial’, Managerial and Decision Economics,vol. 28, no. 4–5, p. 229.

Weissman, R 2007, ‘Big pharma and AIDS: Act II patents and the price of second-line treatment’, Multinational Monitor, vol. 28, no. 2.

WHO 2002a, ‘Promoting rational use of medicines: Core components’,WHO Policy Perspectives on Medicines, no. 5, World Health Organization,Geneva.

———2002b, ‘The selection of essential medicines’, WHO Policy Perspectives onMedicine, no. 4, World Health Organization, Geneva.

———2002c, The World Health Report 2002: Reducing Risks, Promoting Healthy Life,World Health Organization, Geneva.

———2003a, ‘Effective medicines regulation: Ensuring safety, efficacy and qual-ity’, WHO Policy Perspectives on Medicine, no. 7, World Health Organization,Geneva.

———2003b, ‘How to develop and implement a national drug policy’, WHOPolicy Perspectives on Medicine, no. 6, World Health Organization, Geneva.

———2004a, ‘Equitable access to essential medicines: A framework for collectiveaction’, WHO Policy Perspective on Medicines, no. 8, World Health Organization,Geneva.

———2004b, The World Medicines Situation, World Health Organization, Geneva.———2006a, ‘Elements of a global strategy and plan of action, A/PHI/IGWG/

1/4’, Intergovernmental Working Group on Public Health, Innovation andIntellectual Property, World Health Organization, Geneva.

———2006b, The World Health Report 2006: Working Together for Health, WorldHealth Organization, Geneva.

———2007, World Health Report 2007: A Safer Future – Global Public Health Securityin the 21st Century, World Health Organization, Geneva, Switzerland.

WHO/WTO 2001, ‘Report of the workshop on differential pricing and financingof essential drugs’, Hosbjor, Norway, 8–11 April.

Wikipedia 2008, ‘Cipla and the fight against HIV/AIDS in the developing world’,viewed 21 September 2008, http://en.wikipedia.org/wiki/Cipla.

Wilding, I 2002, ‘Injecting innovation into the drug development process’, ScripMagazine, October, pp. 15–6.

World Bank 2002, India: Raising the Sights – Better Health Systems for India’s Poor –Findings, Analysis and Options, World Bank, Washington, DC.

References 313

———2003, The Little Data Book, The World Bank, Washington, DC.———2006, World Development Report: Equity and Development, The World Bank,

Washington, DC.WTO 1994, Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS),

The World Trade Organization, Geneva, 15 April, viewed 12 February 2003,http://www.wto.org/english/docs_e/legal_e/27-trips_01_e.htm.

———2000, Canada: Patent Protection of Pharmaceutical Products, WT/DS114/R,World Trade Organization, Geneva, 17 March, viewed 17 February 2007, http://www.wto.org/english/tratop_e/dispu_e/7428d.pdf.

———2006a, 10 Common Misunderstandings About the WTO, World Trade Organi-zation, Geneva.

———2006b, Compulsory Licensing of Pharmaceuticals and TRIPS, World TradeOrganization, Geneva, viewed 28 May 2007, http://www.wto.org/english/tratop_e/trips_e/public_health_faq_e.htm.

———2010, Understanding the WTO: The Agreements, World Trade Organization,Geneva, viewed 16 March 2010, http://www.wto.org/english/thewto_e/whatis_e/tif_e/agrm1_e.htm.

Wyllie, MG 2005, ‘Evergreening: There’s life in the old drug yet’, British Journal ofUrology, vol. 95, no. 9, 12 May, pp. 1359–60.

Yusuf, A & Moncayo von Hase, A 1992, ‘Intellectual property protection andinternational trade-exhaustion of rights revisited’, World Competition, vol. 16,no. 1, pp. 115–31.

Zutshi, BK 1998, ‘Bring TRIPS into the multilateral trading system’, in J Bhagwati& M Hirsch (eds), The Uruguay Round and Beyond: Essays in Honour of ArthurDunkel, Springer, Berlin, pp. 37–49.

Index

Abbott, F., 19, 95, 97, 187Abegunde, D., 143, 160access to medicines, 1–6, 9, 14, 22, 31,

51–3, 57, 63–7, 76, 81, 85, 97,103–4, 137–8, 141–60, 175–6,180, 184, 190–1, 201–2, 204,211–12, 214, 216, 220–1

Indian population with, 2, 15, 60,117, 125, 132–33, 136, 144

Acharya, A., 134Acquired immune deficiency

syndrome (AIDS), see HIV/AIDSAderibigbe, M., 70Adikibi, O., 70advance purchase commitments

(APC) model, 207adverse drug reactions (ADRs), 44Aggarwal, A., 59, 61Ahuja, R., 134Aiyer, S., 73Alexander, J., 108Alphapharm, 42Alsegård, E., 201alternative models, 201–213Angell, M., 49antiretrovirals (ARVs), 63–5, 81,

203, 205Apotex, 97Arrow Pharmaceuticals, 42Ashton, T., 13, 16AstraZeneca, 50, 59, 66, 71, 75, 97AT Kearney, 69Australia, 25, 71, 87, 92, 131, 183

ageing population, 141generics in, 40–41patient co-payments, 137–9,

149, 154pharmaceutical market, 38, 40private health insurance in, 135trade margins in pharmaceuticals,

120Australian Bureau of Statistics, 141

Australian Institute of Health andWelfare, 161

Austrom, D., 46Ayurvedic, Yoga, Unani, Siddha, and

Homeopathic (AYUSH), 135, 170see also traditional medicines

Babu, G., 78Baker, B., 27Balance, R., 111Balasubramaniam, K., 183Barry, M., 51Barton, J., 202, 204–5, 208–9below poverty line (BPL), 133–5,

141–2, 149, 152, 155Berndt, E., 207Berry, A., 207Bhagat, M., 2, 60–1, 143Bidwai, P., 89Biocon, 75Bisserbe, N., 74Blech, J., 37, 50, 61Blendon, R., 138, 148blockbuster drugs, 34–5, 53, 81,

92, 189Bloomberg, 36Boldrin, M., 177, 179Bower, D., 62, 74, 76Braee, R., 127Bristol-Myers Squibb (BMS), 37, 75,

77, 101Brown, P., 39Bureau of National Affairs, 188

Cai, Q., 111Caplow, T., 92Cefaclor, 80Central Drug Research Institute

(CDRI), 105, 210Chadha, A., 71, 78Chataway, J., 73Chataway, M., 190

314

Index 315

Chaturvedi, K., 105Chaudhuri, S., 1, 59, 62, 95–6,

114, 179Chin, J., 185CIMS, 121, 123Cipla, 59, 64, 92, 97–8,

122Clements, P., 27Clift, C., 101Cole, J., 13–14, 17Collier, R., 47Commission on Intellectual Property

Rights, 192–5Commission on Intellectual Property

Rights Innovation and PublicHealth, 101

Commission on Macroeconomics andHealth, 51

compulsory licensing, 20–4, 84, 86,94–7, 103, 143, 215

Congressional Budget Office (CBO),44–6

contract research and manufacturing(CRAM), 34, 75–9

contract research organizations, 75co-payments, see patient

co-paymentsCornish, W., 24Correa, C., 19, 23–4, 26, 29Council of Scientific and Industrial

Research (CSIR), 108, 110, 219Cruddas, J., 50Cutler, D., 35–6, 39, 43Cygnus, 58, 75

Danzon, P., 36–7, 202Darbourne, A., 203Das, S., 60, 113, 121data exclusivity, see data protectiondata protection, 15, 26–8, 87,

99–103, 109David, P., 12Davis, M., 16–17Deardof, A., 185Deloitte Recap, 36DeNavas-Walt, C., 131, 135Department of Health, 127, 197Department of Health and

Ageing, 129

developing new drugs, 5, 14–16, 32–4,42–4, 50–2, 106

costs of, 46–8process of, 43time to, 44–6

differential patenting model, 203differential pricing model, 202DiMasi, J., 44–5, 47–9disability adjusted life years (DALYs),

204, 207Doha Declaration, 22, 24, 95donating drugs model, 204Dongre, R., 12Drohan, M., 11Douglas Pharmaceuticals, 42Drahos, P., 21, 27, 90, 183, 190Drug Today, 121, 123DRL, see Dr Reddy’sDr Reddy’s, 52, 59, 64, 73, 75drug price controls, 14, 16, 84,

111–17, 131, 136, 219Drug Price Control Order (DPCO),

112, 159of 1970, 112, 114–15of 1979, 70, 112, 115of 1987, 112, 116of 1995, 112–14, 125of 2004, 116–17

Drug Price control models, 126Australia, 127, 129Canada, 128Germany, 128–9New Zealand, 127United Kingdom, 127

Drug prices, 2–4, 14–15, 43, 67, 79, 81,84, 98, 103, 121–6, 143, 146, 188

post-TRIPS changes to, 123–6voluntary reductions to, 121–2

Duckett, S., 129, 141Dukes, G., 33, 47–8Dunkley, G. 10Dutta, A., 182

Economic Research Foundation, 142,168

The Economist, 17, 191Edison, T., 18effective patent life, 45Eli Lilly, 71, 80

316 Index

Elliott, R., 97Ellis, R., 131–3, 137Embassy of the United States, 93Essentialdrugs, 59EurActiv, 28European Commission, 24, 34, 40,

42–3, 89, 92, 110, 192, 198–9European Generic Medicines

Association (EGMA), 16European Federation of

Pharmaceutical Industries andAssociations (EFPIA), 25, 34, 37–8,40, 42, 44, 47

European Parliament, 89ever-greening, 87, 109

see also frivolous claimsexclusive marketing rights (EMRs),

82–4The Expert Committee, 59, 61

Food and Drug Administration (FDA),44, 46, 62, 71, 77, 87, 94, 103

Federal Trade Commission (FTC),195–7

Federation of Indian Chambers ofCommerce and Industry (FICCI),62, 74, 76

Ferreiro, A., 137FierceBiotech, 78Finger, J., 181–2, 184Flink, J., 13Foroohar, R., 207foreign direct investment (FDI), 4–5,

68–72, 217Foreign Exchange Regulation Act

(FERA), 69–70Frank, R., 36frivolous claims, 84, 88–9, 92, 110

Galpalli, N., 58–9Gambardella, A., 43, 47Garg, C., 133, 137Gassmann, O., 34–5, 37, 45, 188Genepharm, 40, 42General Agreement on Tariffs and

Trade (GATT), 5, 9–11, 214General Insurance Corporation of

India, 132Generic Handbook, 39

generics, 3, 15–16, 23–7, 37–42, 57,60, 64, 74–5, 77, 81–3, 85, 92,101–3, 120, 126–30, 180, 188,198, 203–4, 215

GlaxoSmithKline (GSK), 37, 42, 50,71, 75, 91, 115

Glivec, 82, 84Global-Challenges, 64Global Forum for Health Research, 51Global pharmaceutical industry, 2–4,

14, 20, 22, 25, 36–7, 40, 47–50product, 34–5structure, 33–4

Goddard, M., 111, 127Goozner, M., 47–8Government of Australia, 12, 41, 154,

159Government of Canada, 128Government of India, 58–65, 67–9,

71, 76, 78, 81, 83–4, 87, 92, 94,106, 108, 112–13, 116, 120–1,141–3, 147–8, 151–2, 155–8, 161,164–9, 181

Government of the United States,205–6

Grabowski, H., 47–8, 205–6Graf von der Schulenburg, J., 128Gray, A., 111Gupta, A., 60Gupta, I., 132–3

Hansen, R., 47Harten, C., 135, 138Harvey, K., 51, 61, 126Hatch-Waxman Act, 27, 62, 81, 101Hathi Committee Report (HCR), 61,

115, 147Haub, C., 161–3Hawthorne, F., 52, 177–8Hayek, F., 17health expenditure, 38, 52, 130–1, 139

private, 5, 39, 142, 155–9, 166–71,220

public, 142, 156–9, 166, 222health impact fund (HIF) model, 210health insurance, 6, 39, 118, 128,

131–40, 166in India, 131–5; private, 135–7

Heinen, C., 72, 76

Index 317

Henry, D., 146Hertz, A., 11Hesse, C., 12Hexal Australia, 42Hiddleston, S., 87High Court, 83, 89, 93, 97–8, 104HIV/AIDS, 63–5, 81–2, 91, 97–8,

114–25, 188, 203Hoekman, B., 10Hofstede, G., 13Hollis, A., 206, 210Hope, J., 13House of Commons Health

Committee, 87, 89, 197–8Hughes, J., 188Humer, F., 33

Ibrahim, M., 136incremental value based rewards

model, 206IDR, 121, 123IMS Health, 87IndiaHealth model, 144–58

benefits of, 159–60costing of, 161–8funding, 168–70implementing, 147out-of-pocket expenditure under,

155–9structure of, 170

India Patent Act, 13–14, 28, 59, 70,84–7, 89, 92–3, 95–7, 99, 105,109, 115, 178–9, 194, 196

Appellate Board, 90, 99impact of, 81–5, 103provisions to oppose, 90–8uncertainties and ambiguities

under, 99–108Indian pharmaceutical industry,

58–62, 77, 79–80, 159business models, 4, 72–8, 218development of, 57–61exports, 61–2; impact of TRIPS on,

63–7, 72, 216foreign acquisitions by, 77–8imports, 61, 68new drugs, 191product, 58small scale units, 59–61

Indian pharmaceutical market, 58–61India population, 141–5, 148–9,

151–66, 169–71insurance, see health insuranceintellectual property rights (IPRs),

10–14, 20, 69–70, 79, 89, 101,111, 182, 192–3, 200

case for, 13–16case against, 16–19see also patents

Inter-Ministerial ConsultativeCommittee (IMCC), 102–3

International Federation ofPharmaceutical ManufacturersAssociations (IFPMA), 101, 188

International Monetary Fund (IMF),167–9

INHATA, 147Insurance Regulatory and

Development Authority (IRDA),136

IP-Watch, 91

Jack, W., 182Jatania, P., 82Jefferson, T., 17Jeremy, D., 177Jorge, M., 19, 183Jyothi-Datta, P., 91

Kamath, G., 40, 64, 75, 78Kassirer, J., 50Kaul, S., 78Keayla, B., 103Khan, B., 13, 15Khosla, R., 191Klein, N., 23Knowledge@Wharton, 151Koshy, S., 24KPMG, 76Kremer, M., 190, 203–5, 207Kumar, R., 89, 105, 177

Labonte, R., 51Lacetera, N., 33Lalitha, N., 80Lall, S., 112Lanjouw, J., 80–1, 115, 179–80, 182,

203–4

318 Index

Lehman, B., 11, 14–15, 190–1least developed countries (LDCs), 96,

98, 179, 215Levine, D., 177, 179Lewis, G., 37Lichtenberg, F., 187, 189Light, D., 207Lippoldt, D., 69Lleras-Muney, A., 189Lloyd, I., 45Lofgren, H., 41, 207low- and middle income countries

(LMICs), 57, 65, 67, 72, 79

Macdonald, S., 180Machlup, F., 12–13, 18Madanmohan, T., 72Mahal, A., 136, 168Malhotra, P., 9, 26, 65–6, 81, 101, 108Managing Intellectual Property, 91Mansfield, E., 14, 69Mashelkar, R., 286Maskus, K., 9, 69, 209Mathew, J., 77, 98Mathew, T., 38Mathieu, M., 46, 50May, C., 12Mayne, R., 14, 32Mazumdar-Shaw, K. 75, 105McEwan, J., 92McLachlan, A., 61Medecin Sans Frontiere (MSF), 82,

91, 101Medicines Australia, 34Medicines and Healthcare Products

Regulatory Agency (MHRA),62, 77

Medico Friends Circle, 60–1MedIndia, 99Melethil, S., 18Merck, 37, 39, 52, 205minimum patenting model, 211Minwalla, S., 61Misra, R., 143, 190Mokyr, J., 16Morag-Sela, T., 27Moran, M., 191, 208Mueller, J., 90, 95, 99Mukherjee, S., 71

Mukreja, D., 64multinational corporations (MNCs),

4–5, 11, 13, 23, 32–4, 51, 59,62–3, 68, 71–4, 79, 89, 94, 97,101, 105, 107, 114–15, 175, 178,180, 182, 184–5, 187, 203, 210

Murray, C., 51mX, 115

Nagendranath, A., 132Nanda, N., 34, 57, 143Nard, C., 12Narrain, S., 82, 113, 117Narula, R., 83National Academies Board on Science

Technology and Economic Policy,197

National Commission onMacroeconomics and Health(NCMH), 117

National Essential Drugs List, 117National Institute of Pharmaceutical

Education and Research (NIPER),125

National Institute of ScienceTechnology and DevelopmentStudies (NISTADS), 94, 104, 106–7

National Institutes of Health (NIH),16, 43, 49–50

National List of Essential Medicines(NLEM), 114, 117–18, 125

National ManufacturingCompetitiveness Council(NMCC), 117

National Pharmaceutical PricingAuthority (NPPA), 116, 118, 130,146

Nicolas Piramal, 59, 60, 65, 101, 106Nordmann, R., 190North, D., 14Novartis, 71, 82, 89, 110, 195Nunnenkamp, P., 69

OneIndia, 135open access model, 208Organisation for Economic

Co-operation and Development(OECD), 32–3, 35, 37–8, 40, 50,62, 130

Index 319

Organisation of PharmaceuticalProducers of India (OPPI), 57, 59

Orphan Drugs Act as a model, 205Outterson, K., 26Oxfam, 182, 184

Palit, A., 70, 72Pammolli, F., 285parallel imports, 22, 24–5, 30, 143, 215parallel trade, 202, 204Patent Lens, 183patents, 11–21, 23–30, 33–4, 36, 38,

40–2, 52, 59, 63, 65–8, 80–110,118–19, 127–8, 176, 195–7, 203,215, 217–19, 222–4

in developed countries, 176in pharmaceutical products, 177–80see also intellectual property rights

(IPRs)patient co-payments, 137–40, 155–9Patnaik, U., 286Perlitz, U., 61Pettypiece, S., 190Pfizer, 35–7, 45, 48, 59, 71, 91, 97,

108, 115, 175–6, 190Phadke, A., 68Pharmaceutical Benefits Scheme (PBS),

40–2, 129, 131, 138–9, 183Pharmaceutical & Drug

Manufacturers, 58pharmaceutical innovation, 11–17,

29, 33–4, 42–4, 47, 50, 59, 73,80–1, 84, 87, 104–9, 189, 218

pharmaceutical marketing, 17, 25–7,34–5, 43–4, 47, 50–1, 57, 61, 73–5,82–3, 90–4

pharmaceutical markets, 37–42pharmaceutical patents investigated,

192–200see also patents

pharmaceutical research anddevelopment, 16, 32–4, 42–3,45–6, 48–9, 51, 106, 189, 197,202–8

Pharmaceutical Research andManufacturers of America(PhRMA), 14–16, 28, 39–40, 46,49, 175–6, 217

pharmaceutical trade margins, 119–20

Pogge, T., 184Posner, R., 17, 176Pradhan, S., 58, 60Prahalad, C., 74President’s Ordinance, 84, 90price controls, see drug price controlsPublic Citizen, 49public good, 21, 209public health expenditure, see health

expenditurePublic-Private Partnerships (PPPs)

model, 207Pugatch, M., 101

Ram, P., 85, 94–5, 107Ranbaxy, 36, 59, 64, 74–5, 77, 80, 83,

98, 106, 122Rangnekar, D., 80Raymus, P., 142, 168reference pricing, 119, 126–7Reichman, J., 11, 19, 209Reserve Bank of India (RBI), 69,

73, 142Rhein, R., 183Roche, 33, 91, 97–8Rogers, A., 179Roumeliotis, G., 68Roy, N., 61Ruston, G., 12

Sachs, J., 185Sager, A., 38Sakthivel, S., 120, 123–4The Sandhu Committee, 117–20Sanofi-Aventis, 50, 71Santerre, R., 131, 188Sauer, C., 100Saunders, P., 205Scherer, F., 24, 178, 186–87, 189Schiff, E., 178Schneider, F., 70Schreyoegg, J., 129Schweitzer, S., 32Scott, A., 35Scrip, 73Scrip News, 35, 50, 61, 208Sen, A., 185The Sen Committee, 61, 116,

118–20, 129

320 Index

The Seth Committee, 117Seyoum, B., 69–70Shadlen, K., 27, 73Shah, D., 59, 69–70Shiva, V., 19Singh, K., 97Singleton, A., 17Sketris, I., 128Smith, S., 69So, A., 101Solow, R., 13Special 301, 101, 183Srinivasan, S., 104Stiglitz, J., 17, 180, 186Stoate, N., 15–16Swain, N., 58Sweeny, K., 40–41, 120

Tagamet, 34, 92, 189Tamilnadu Pharmaceutical Sciences

Welfare Trust, 94Taxol, 101Taylor, P., 78test data, 198

see also data protectionTherapeutic Goods Administration

(TGA), 62, 77, 129traditional medicines, 135, 148,

159–60, 171see also Ayurvedic, Yoga, Unani,

Siddha, and Homeopathic(AYUSH)

Therapeutic Goods Act, 92Timmermans, K., 101Torbet, J., 191trade margins, see pharmaceutical

trade marginsTrade Related Aspects of Intellectual

Property Rights (TRIPS), 9–10, 15,19, 70, 94–5, 100, 104, 111, 143,176–80, 222–4

appropriateness of, 175–200, 222–24Articles, 20, 25, 28–9, 96Bolar exemption, 15–16, 25–6, 85,

103costs and benefits of, 180; to

developed countries, 183; to

developing countries, 180–3,184–92

flexibilities, 10, 21–2, 25–6, 94–5,98, 215

The Tribune, 120TRIPS-plus, 20, 26, 179, 215tropical diseases, 14, 32, 51–2, 72, 79,

114, 160, 187, 189–91, 204, 206,210, 224

tuberculosis, 51, 64, 71, 108, 190

United Nations, 151, 161–5United Nations Centre on

Transnational Corporations(UNCTC), 70

United Nations Conference on Tradeand Development (UNCTAD), 71

United Nations DevelopmentProgramme (UNDP), 20, 176

Uruguay Round, 9, 181, 183United States-Australia Free Trade

Agreement, 92, 183

Verband der ForschenderArzeneimittelhersteller, 128

Verheugen, G., 15Vernon, J., 48

Watal, J., 24Weissman, R., 64The Wharton School, 63Wikipedia, 64Wilding, I., 44Wockhardt, 59, 65, 77, 91, 106, 122World Bank, 17, 69–70, 143, 181, 202World Health Organization (WHO),

59–60, 62, 114, 117, 127, 142–3,146, 190, 202, 205

World Trade Organization (WTO),9–11, 19, 22–3, 25–7, 68, 70, 82,86, 94, 96–7, 104–5, 179, 181–6,201, 209, 214–15

Wyllie, M., 195

Yusuf, A., 24

Zidovudine, 66, 87, 91Zutshi, B., 10, 30