Glenmark Pharmaceuticals Discontinued
FDA Approved Drugs

Glenmark Pharmaceuticals Discontinued

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 22
  • Latest Approval Date May 10, 2019
  • Data Source FDA
  • First Approval Date Feb 05, 1991
All
84
View
Unclassified
5
View
Discontinued
22
View
OTC
10
View
RX
47
View
Company Overview

Company

Glenmark Pharmaceuticals Discontinued

Country

India

Website

Visit Website

Email

india_marketing@glenmarkpharma.com

Social Profiles

Company Snapshot

Glenmark Pharmaceuticals Discontinued

Glenmark House, B. D. Sawant Marg, Chakala, Off Western Express Highway, Andheri (E), Mumbai - 400 099

India

www.glenmarkpharma.com/ india_marketing@glenmarkpharma.com View on Map
FDA Approved Drug Records ( 22 records )
2008
23 Sep
Discontinued Application: 78930

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

2008-09-23

78930 / 1

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

78930

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

2008-09-23

Regulatory Status

Discontinued

2017
20 Mar
Discontinued Application: 208933

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-03-20

208933 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

208933

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-03-20

Regulatory Status

Discontinued

2018
26 Mar
Discontinued Application: 209004

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-03-26

209004 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

209004

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-03-26

Regulatory Status

Discontinued

2018
10 May
Discontinued Application: 209095

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-05-10

209095 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

209095

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-05-10

Regulatory Status

Discontinued

2015
30 Oct
Discontinued Application: 202894

Drug Name

CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE;1%

Approval Date

2015-10-30

202894 / 1

Active Ingredient

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Application Number

202894

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE;1%

Approval Date

2015-10-30

Regulatory Status

Discontinued

2017
26 Sep
Discontinued Application: 209494

Drug Name

DESONIDE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-09-26

209494 / 1

Active Ingredient

DESONIDE

Application Number

209494

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-09-26

Regulatory Status

Discontinued

2017
24 Jul
Discontinued Application: 209729

Drug Name

DESONIDE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-07-24

209729 / 1

Active Ingredient

DESONIDE

Application Number

209729

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-07-24

Regulatory Status

Discontinued

1991
05 Feb
Discontinued Application: 88999

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1991-02-05

88999 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

88999

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1991-02-05

Regulatory Status

Discontinued

1991
05 Feb
Discontinued Application: 89000

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1991-02-05

89000 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

89000

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1991-02-05

Regulatory Status

Discontinued

1991
05 Feb
Discontinued Application: 89001

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1991-02-05

89001 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

89001

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1991-02-05

Regulatory Status

Discontinued

2019
10 May
Discontinued Application: 209495

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-05-10

209495 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

209495

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-05-10

Regulatory Status

Discontinued

2019
10 May
Discontinued Application: 209495

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2019-05-10

209495 / 2

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

209495

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2019-05-10

Regulatory Status

Discontinued

2010
17 Mar
Discontinued Application: 90718

Drug Name

MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;7.5MG

Approval Date

2010-03-17

90718 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Application Number

90718

Product Number

1

Dosage Form

-

Strength

12.5MG;7.5MG

Approval Date

2010-03-17

Regulatory Status

Discontinued

2010
17 Mar
Discontinued Application: 90718

Drug Name

MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;15MG

Approval Date

2010-03-17

90718 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Application Number

90718

Product Number

2

Dosage Form

-

Strength

12.5MG;15MG

Approval Date

2010-03-17

Regulatory Status

Discontinued

2010
17 Mar
Discontinued Application: 90718

Drug Name

MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;15MG

Approval Date

2010-03-17

90718 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Application Number

90718

Product Number

3

Dosage Form

-

Strength

25MG;15MG

Approval Date

2010-03-17

Regulatory Status

Discontinued

2008
28 May
Discontinued Application: 78541

Drug Name

MOMETASONE FUROATE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-05-28

78541 / 1

Active Ingredient

MOMETASONE FUROATE

Application Number

78541

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-05-28

Regulatory Status

Discontinued

2008
28 May
Discontinued Application: 78571

Drug Name

MOMETASONE FUROATE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-05-28

78571 / 1

Active Ingredient

MOMETASONE FUROATE

Application Number

78571

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-05-28

Regulatory Status

Discontinued

2011
15 Jul
Discontinued Application: 90618

Drug Name

NIZATIDINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2011-07-15

90618 / 1

Active Ingredient

NIZATIDINE

Application Number

90618

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2011-07-15

Regulatory Status

Discontinued

2011
15 Jul
Discontinued Application: 90618

Drug Name

NIZATIDINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-07-15

90618 / 2

Active Ingredient

NIZATIDINE

Application Number

90618

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-07-15

Regulatory Status

Discontinued

2008
19 Nov
Discontinued Application: 78542

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2008-11-19

78542 / 1

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

78542

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2008-11-19

Regulatory Status

Discontinued

2008
19 Nov
Discontinued Application: 78542

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2008-11-19

78542 / 2

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

78542

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2008-11-19

Regulatory Status

Discontinued

2017
22 Aug
Discontinued Application: 208320

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2017-08-22

208320 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

208320

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2017-08-22

Regulatory Status

Discontinued

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Drug Status Breakdown
22 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

BETAMETHASONE DIPROPIONATE

Application Number

78930

Product Number

1

Active Ingredient

BETAMETHASONE DIPROPIONATE

Dosage Form

-

Strength

EQ 0.05% BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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