Taro Pharmaceutical Industries Discontinued
FDA Approved Drugs

Taro Pharmaceutical Industries 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 83
  • Latest Approval Date Jun 28, 2024
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
209
View
Unclassified
1
View
Discontinued
83
View
OTC
17
View
RX
108
View
Company Overview

Company

Taro Pharmaceutical Industries Discontinued

Country

U.S.A

Website

Visit Website

Email

enquiries@pharmacompass.com

Social Profiles

Company Snapshot

Taro Pharmaceutical Industries Discontinued

Three Skyline Drive Hawthorne, NY 10532

U.S.A

www.taro.com/ enquiries@pharmacompass.com View on Map
FDA Approved Drug Records ( 83 records )
1982
18 Nov
Discontinued Application: 62405

Drug Name

A/T/S

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-11-18

62405 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62405

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-11-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18337

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18337 / 1

Active Ingredient

ACETAMINOPHEN

Application Number

18337

Product Number

1

Dosage Form

-

Strength

650MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

2023
24 Mar
Discontinued Application: 214458

Drug Name

AMINOCAPROIC ACID

Product Number

1

Dosage Form

-

Strength

0.25GM/ML

Approval Date

2023-03-24

214458 / 1

Active Ingredient

AMINOCAPROIC ACID

Application Number

214458

Product Number

1

Dosage Form

-

Strength

0.25GM/ML

Approval Date

2023-03-24

Regulatory Status

Discontinued

2002
29 Nov
Discontinued Application: 76362

Drug Name

AMIODARONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2002-11-29

76362 / 1

Active Ingredient

AMIODARONE HYDROCHLORIDE

Application Number

76362

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2002-11-29

Regulatory Status

Discontinued

2003
02 Dec
Discontinued Application: 76362

Drug Name

AMIODARONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2003-12-02

76362 / 2

Active Ingredient

AMIODARONE HYDROCHLORIDE

Application Number

76362

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2003-12-02

Regulatory Status

Discontinued

2019
11 Dec
Discontinued Application: 211521

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML

Approval Date

2019-12-11

211521 / 1

Active Ingredient

AZITHROMYCIN

Application Number

211521

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML

Approval Date

2019-12-11

Regulatory Status

Discontinued

2017
27 Feb
Discontinued Application: 205112

Drug Name

BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

2MG/5ML;10MG/5ML;30MG/5ML

Approval Date

2017-02-27

205112 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

205112

Product Number

1

Dosage Form

-

Strength

2MG/5ML;10MG/5ML;30MG/5ML

Approval Date

2017-02-27

Regulatory Status

Discontinued

2000
21 Dec
Discontinued Application: 75875

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2000-12-21

75875 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

75875

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2000-12-21

Regulatory Status

Discontinued

2013
21 Jun
Discontinued Application: 201106

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-06-21

201106 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

201106

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-06-21

Regulatory Status

Discontinued

2013
21 Jun
Discontinued Application: 201106

Drug Name

CARBAMAZEPINE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2013-06-21

201106 / 2

Active Ingredient

CARBAMAZEPINE

Application Number

201106

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2013-06-21

Regulatory Status

Discontinued

2013
21 Jun
Discontinued Application: 201106

Drug Name

CARBAMAZEPINE

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2013-06-21

201106 / 3

Active Ingredient

CARBAMAZEPINE

Application Number

201106

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2013-06-21

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77780

Drug Name

CARVEDILOL

Product Number

1

Dosage Form

-

Strength

3.125MG

Approval Date

2007-09-05

77780 / 1

Active Ingredient

CARVEDILOL

Application Number

77780

Product Number

1

Dosage Form

-

Strength

3.125MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77780

Drug Name

CARVEDILOL

Product Number

2

Dosage Form

-

Strength

6.25MG

Approval Date

2007-09-05

77780 / 2

Active Ingredient

CARVEDILOL

Application Number

77780

Product Number

2

Dosage Form

-

Strength

6.25MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77780

Drug Name

CARVEDILOL

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2007-09-05

77780 / 3

Active Ingredient

CARVEDILOL

Application Number

77780

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77780

Drug Name

CARVEDILOL

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

2007-09-05

77780 / 4

Active Ingredient

CARVEDILOL

Application Number

77780

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2009
22 Jul
Discontinued Application: 78072

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-07-22

78072 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78072

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-07-22

Regulatory Status

Discontinued

2009
22 Jul
Discontinued Application: 78072

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2009-07-22

78072 / 3

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78072

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2009-07-22

Regulatory Status

Discontinued

2009
22 Jul
Discontinued Application: 78072

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES RELIEF

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2009-07-22

78072 / 2

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78072

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2009-07-22

Regulatory Status

Discontinued

2009
22 Jul
Discontinued Application: 78072

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES RELIEF

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2009-07-22

78072 / 4

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78072

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2009-07-22

Regulatory Status

Discontinued

2004
06 Oct
Discontinued Application: 76912

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-10-06

76912 / 2

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76912

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-10-06

Regulatory Status

Discontinued

2004
06 Oct
Discontinued Application: 76912

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-10-06

76912 / 3

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76912

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-10-06

Regulatory Status

Discontinued

2004
06 Oct
Discontinued Application: 76912

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-10-06

76912 / 4

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76912

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-10-06

Regulatory Status

Discontinued

2006
22 Mar
Discontinued Application: 77278

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-03-22

77278 / 1

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77278

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-03-22

Regulatory Status

Discontinued

2006
22 Mar
Discontinued Application: 77278

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-03-22

77278 / 2

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77278

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-03-22

Regulatory Status

Discontinued

2006
22 Mar
Discontinued Application: 77278

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-03-22

77278 / 3

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77278

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-03-22

Regulatory Status

Discontinued

2018
22 Oct
Discontinued Application: 209440

Drug Name

CLOBAZAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2018-10-22

209440 / 1

Active Ingredient

CLOBAZAM

Application Number

209440

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2018-10-22

Regulatory Status

Discontinued

2018
22 Oct
Discontinued Application: 209440

Drug Name

CLOBAZAM

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2018-10-22

209440 / 2

Active Ingredient

CLOBAZAM

Application Number

209440

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2018-10-22

Regulatory Status

Discontinued

2024
14 Mar
Discontinued Application: 208563

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2024-03-14

208563 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

208563

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2024-03-14

Regulatory Status

Discontinued

2019
01 Mar
Discontinued Application: 209430

Drug Name

DAPSONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2019-03-01

209430 / 1

Active Ingredient

DAPSONE

Application Number

209430

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2019-03-01

Regulatory Status

Discontinued

2019
01 Mar
Discontinued Application: 209430

Drug Name

DAPSONE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2019-03-01

209430 / 2

Active Ingredient

DAPSONE

Application Number

209430

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2019-03-01

Regulatory Status

Discontinued

2015
30 Jun
Discontinued Application: 202592

Drug Name

DESLORATADINE

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

2015-06-30

202592 / 1

Active Ingredient

DESLORATADINE

Application Number

202592

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

2015-06-30

Regulatory Status

Discontinued

2020
01 Jul
Discontinued Application: 213063

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2020-07-01

213063 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

213063

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2020-07-01

Regulatory Status

Discontinued

2020
01 Jul
Discontinued Application: 213063

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2020-07-01

213063 / 2

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

213063

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2020-07-01

Regulatory Status

Discontinued

2020
01 Jul
Discontinued Application: 213063

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2020-07-01

213063 / 3

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

213063

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2020-07-01

Regulatory Status

Discontinued

2020
01 Jul
Discontinued Application: 213063

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2020-07-01

213063 / 4

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

213063

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2020-07-01

Regulatory Status

Discontinued

2020
01 Jul
Discontinued Application: 213063

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2020-07-01

213063 / 5

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

213063

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2020-07-01

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76507

Drug Name

FLUCONAZOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

76507 / 1

Active Ingredient

FLUCONAZOLE

Application Number

76507

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76507

Drug Name

FLUCONAZOLE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

76507 / 2

Active Ingredient

FLUCONAZOLE

Application Number

76507

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76507

Drug Name

FLUCONAZOLE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

76507 / 3

Active Ingredient

FLUCONAZOLE

Application Number

76507

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76507

Drug Name

FLUCONAZOLE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

76507 / 4

Active Ingredient

FLUCONAZOLE

Application Number

76507

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2013
03 Jul
Discontinued Application: 76672

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

2013-07-03

76672 / 1

Active Ingredient

GABAPENTIN

Application Number

76672

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

2013-07-03

Regulatory Status

Discontinued

2013
02 Aug
Discontinued Application: 77261

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-08-02

77261 / 1

Active Ingredient

GABAPENTIN

Application Number

77261

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-08-02

Regulatory Status

Discontinued

2013
02 Aug
Discontinued Application: 77261

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2013-08-02

77261 / 2

Active Ingredient

GABAPENTIN

Application Number

77261

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2013-08-02

Regulatory Status

Discontinued

2013
02 Aug
Discontinued Application: 77261

Drug Name

GABAPENTIN

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2013-08-02

77261 / 3

Active Ingredient

GABAPENTIN

Application Number

77261

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2013-08-02

Regulatory Status

Discontinued

2010
28 May
Discontinued Application: 90817

Drug Name

GRANISETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2010-05-28

90817 / 1

Active Ingredient

GRANISETRON HYDROCHLORIDE

Application Number

90817

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2010-05-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86154

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

86154 / 1

Active Ingredient

HYDROCORTISONE

Application Number

86154

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86155

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86155 / 1

Active Ingredient

HYDROCORTISONE

Application Number

86155

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86256

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

86256 / 1

Active Ingredient

HYDROCORTISONE

Application Number

86256

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
12 Feb
Discontinued Application: 89024

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1986-02-12

89024 / 1

Active Ingredient

HYDROCORTISONE

Application Number

89024

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1986-02-12

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2019-07-22

207098 / 1

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2019-07-22

207098 / 2

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2019-07-22

207098 / 3

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

4

Dosage Form

-

Strength

6MG

Approval Date

2019-07-22

207098 / 4

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

4

Dosage Form

-

Strength

6MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

5

Dosage Form

-

Strength

8MG

Approval Date

2019-07-22

207098 / 5

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

5

Dosage Form

-

Strength

8MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

6

Dosage Form

-

Strength

10MG

Approval Date

2019-07-22

207098 / 6

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

6

Dosage Form

-

Strength

10MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2019
22 Jul
Discontinued Application: 207098

Drug Name

ILOPERIDONE

Product Number

7

Dosage Form

-

Strength

12MG

Approval Date

2019-07-22

207098 / 7

Active Ingredient

ILOPERIDONE

Application Number

207098

Product Number

7

Dosage Form

-

Strength

12MG

Approval Date

2019-07-22

Regulatory Status

Discontinued

2009
04 Feb
Discontinued Application: 79204

Drug Name

LAMOTRIGINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-02-04

79204 / 1

Active Ingredient

LAMOTRIGINE

Application Number

79204

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-02-04

Regulatory Status

Discontinued

2009
04 Feb
Discontinued Application: 79204

Drug Name

LAMOTRIGINE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-02-04

79204 / 2

Active Ingredient

LAMOTRIGINE

Application Number

79204

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2009-02-04

Regulatory Status

Discontinued

2010
01 Feb
Discontinued Application: 78960

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2010-02-01

78960 / 1

Active Ingredient

LEVETIRACETAM

Application Number

78960

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

2010-02-01

Regulatory Status

Discontinued

2010
01 Feb
Discontinued Application: 78960

Drug Name

LEVETIRACETAM

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2010-02-01

78960 / 2

Active Ingredient

LEVETIRACETAM

Application Number

78960

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2010-02-01

Regulatory Status

Discontinued

2010
01 Feb
Discontinued Application: 78960

Drug Name

LEVETIRACETAM

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2010-02-01

78960 / 3

Active Ingredient

LEVETIRACETAM

Application Number

78960

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2010-02-01

Regulatory Status

Discontinued

2010
01 Feb
Discontinued Application: 78960

Drug Name

LEVETIRACETAM

Product Number

4

Dosage Form

-

Strength

250MG

Approval Date

2010-02-01

78960 / 4

Active Ingredient

LEVETIRACETAM

Application Number

78960

Product Number

4

Dosage Form

-

Strength

250MG

Approval Date

2010-02-01

Regulatory Status

Discontinued

2013
26 Jul
Discontinued Application: 202673

Drug Name

LEVOCETIRIZINE DIHYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG/5ML

Approval Date

2013-07-26

202673 / 1

Active Ingredient

LEVOCETIRIZINE DIHYDROCHLORIDE

Application Number

202673

Product Number

1

Dosage Form

-

Strength

2.5MG/5ML

Approval Date

2013-07-26

Regulatory Status

Discontinued

2006
07 Nov
Discontinued Application: 78102

Drug Name

MELOXICAM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-11-07

78102 / 1

Active Ingredient

MELOXICAM

Application Number

78102

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-11-07

Regulatory Status

Discontinued

2006
07 Nov
Discontinued Application: 78102

Drug Name

MELOXICAM

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-11-07

78102 / 2

Active Ingredient

MELOXICAM

Application Number

78102

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-11-07

Regulatory Status

Discontinued

2011
23 May
Discontinued Application: 200998

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-05-23

200998 / 1

Active Ingredient

MEPROBAMATE

Application Number

200998

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-05-23

Regulatory Status

Discontinued

2011
23 May
Discontinued Application: 200998

Drug Name

MEPROBAMATE

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2011-05-23

200998 / 2

Active Ingredient

MEPROBAMATE

Application Number

200998

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2011-05-23

Regulatory Status

Discontinued

2006
20 Jun
Discontinued Application: 77965

Drug Name

NORTRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

2006-06-20

77965 / 1

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

77965

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

2006-06-20

Regulatory Status

Discontinued

1988
29 Feb
Discontinued Application: 62876

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1988-02-29

62876 / 1

Active Ingredient

NYSTATIN

Application Number

62876

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1988-02-29

Regulatory Status

Discontinued

2007
30 Nov
Discontinued Application: 77009

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/5ML

Approval Date

2007-11-30

77009 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77009

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/5ML

Approval Date

2007-11-30

Regulatory Status

Discontinued

2011
28 Mar
Discontinued Application: 77729

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2011-03-28

77729 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77729

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2011-03-28

Regulatory Status

Discontinued

2011
28 Mar
Discontinued Application: 77729

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2011-03-28

77729 / 2

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77729

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2011-03-28

Regulatory Status

Discontinued

2011
28 Mar
Discontinued Application: 77729

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2011-03-28

77729 / 3

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77729

Product Number

3

Dosage Form

-

Strength

EQ 24MG BASE

Approval Date

2011-03-28

Regulatory Status

Discontinued

1982
02 Aug
Discontinued Application: 18613

Drug Name

OVIDE

Product Number

1

Dosage Form

-

Strength

0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-08-02

18613 / 1

Active Ingredient

MALATHION

Application Number

18613

Product Number

1

Dosage Form

-

Strength

0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-08-02

Regulatory Status

Discontinued

2024
28 Jun
Discontinued Application: 207498

Drug Name

PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID

Product Number

1

Dosage Form

-

Strength

4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

Approval Date

2024-06-28

207498 / 1

Active Ingredient

ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

Application Number

207498

Product Number

1

Dosage Form

-

Strength

4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

Approval Date

2024-06-28

Regulatory Status

Discontinued

2021
16 Nov
Discontinued Application: 215522

Drug Name

SILDENAFIL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2021-11-16

215522 / 1

Active Ingredient

SILDENAFIL CITRATE

Application Number

215522

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2021-11-16

Regulatory Status

Discontinued

2006
11 Aug
Discontinued Application: 77393

Drug Name

STERILE WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

2006-08-11

77393 / 1

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

77393

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

2006-08-11

Regulatory Status

Discontinued

2003
26 Sep
Discontinued Application: 76525

Drug Name

TERIL

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2003-09-26

76525 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

76525

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2003-09-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17856

Drug Name

TOPICORT

Product Number

1

Dosage Form

-

Strength

0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17856 / 1

Active Ingredient

DESOXIMETASONE

Application Number

17856

Product Number

1

Dosage Form

-

Strength

0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
29 Mar
Discontinued Application: 18586

Drug Name

TOPICORT

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-03-29

18586 / 1

Active Ingredient

DESOXIMETASONE

Application Number

18586

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-03-29

Regulatory Status

Discontinued

1983
30 Sep
Discontinued Application: 18763

Drug Name

TOPICORT

Product Number

1

Dosage Form

-

Strength

0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-09-30

18763 / 1

Active Ingredient

DESOXIMETASONE

Application Number

18763

Product Number

1

Dosage Form

-

Strength

0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-09-30

Regulatory Status

Discontinued

1996
07 Jun
Discontinued Application: 74286

Drug Name

TOPICORT

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1996-06-07

74286 / 1

Active Ingredient

DESOXIMETASONE

Application Number

74286

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1996-06-07

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18309

Drug Name

TOPICORT LP

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18309 / 1

Active Ingredient

DESOXIMETASONE

Application Number

18309

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
83 total
  • Discontinued
Official Source

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

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

Drug Name

A/T/S

Application Number

62405

Product Number

1

Active Ingredient

ERYTHROMYCIN

Dosage Form

-

Strength

2%

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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