DURAMED PHARMS BARR
FDA Approved Drugs

DURAMED PHARMS BARR

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 RX Unclassified
  • Total Records 86
  • Latest Approval Date Feb 24, 2004
  • Data Source FDA
  • First Approval Date Apr 21, 1982
All
86
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Unclassified
2
View
Discontinued
78
View
RX
6
View
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DURAMED PHARMS BARR

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DURAMED PHARMS BARR

Two Quaker Road Pomona, NY 10970

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FDA Approved Drug Records ( 86 records )
1997
18 Nov
Discontinued Application: 40223

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1997-11-18

40223 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

40223

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1997-11-18

Regulatory Status

Discontinued

1997
18 Nov
Discontinued Application: 40223

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

2

Dosage Form

-

Strength

300MG;30MG

Approval Date

1997-11-18

40223 / 2

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

40223

Product Number

2

Dosage Form

-

Strength

300MG;30MG

Approval Date

1997-11-18

Regulatory Status

Discontinued

1997
18 Nov
Discontinued Application: 40223

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

3

Dosage Form

-

Strength

300MG;60MG

Approval Date

1997-11-18

40223 / 3

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

40223

Product Number

3

Dosage Form

-

Strength

300MG;60MG

Approval Date

1997-11-18

Regulatory Status

Discontinued

1984
06 Feb
Discontinued Application: 88353

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1984-02-06

88353 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88353

Product Number

1

Dosage Form

-

Strength

300MG;15MG

Approval Date

1984-02-06

Regulatory Status

Discontinued

1984
06 Feb
Discontinued Application: 88354

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1984-02-06

88354 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88354

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1984-02-06

Regulatory Status

Discontinued

1984
06 Feb
Discontinued Application: 88355

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1984-02-06

88355 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

88355

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1984-02-06

Regulatory Status

Discontinued

1983
31 Mar
Discontinued Application: 88182

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-03-31

88182 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

88182

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-03-31

Regulatory Status

Discontinued

1983
31 Mar
Discontinued Application: 88183

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-03-31

88183 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

88183

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-03-31

Regulatory Status

Discontinued

2001
30 Apr
Discontinued Application: 75796

Drug Name

AVIANE-21

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2001-04-30

75796 / 2

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75796

Product Number

2

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2001-04-30

Regulatory Status

Discontinued

2001
30 Apr
RX Application: 75796

Drug Name

AVIANE-28

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2001-04-30

75796 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75796

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2001-04-30

Regulatory Status

RX

1982
21 Apr
Discontinued Application: 18405

Drug Name

AYGESTIN

Product Number

1

Dosage Form

-

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-04-21

18405 / 1

Active Ingredient

NORETHINDRONE ACETATE

Application Number

18405

Product Number

1

Dosage Form

-

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-04-21

Regulatory Status

Discontinued

1986
14 Aug
Discontinued Application: 71101

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1986-08-14

71101 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

71101

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1986-08-14

Regulatory Status

Discontinued

1986
14 Aug
Discontinued Application: 71102

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1986-08-14

71102 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

71102

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

1986-08-14

Regulatory Status

Discontinued

1986
14 Aug
Discontinued Application: 71103

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1986-08-14

71103 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

71103

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

1986-08-14

Regulatory Status

Discontinued

2001
30 Nov
RX Application: 75840

Drug Name

CRYSELLE

Product Number

1

Dosage Form

-

Strength

0.03MG;0.3MG

Approval Date

2001-11-30

75840 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORGESTREL

Application Number

75840

Product Number

1

Dosage Form

-

Strength

0.03MG;0.3MG

Approval Date

2001-11-30

Regulatory Status

RX

2001
30 Nov
RX Application: 75840

Drug Name

CRYSELLE

Product Number

2

Dosage Form

-

Strength

0.03MG;0.3MG

Approval Date

2001-11-30

75840 / 2

Active Ingredient

ETHINYL ESTRADIOL; NORGESTREL

Application Number

75840

Product Number

2

Dosage Form

-

Strength

0.03MG;0.3MG

Approval Date

2001-11-30

Regulatory Status

RX

1983
25 Oct
Discontinued Application: 88232

Drug Name

CYPROHEPTADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1983-10-25

88232 / 1

Active Ingredient

CYPROHEPTADINE HYDROCHLORIDE

Application Number

88232

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1983-10-25

Regulatory Status

Discontinued

1999
12 Aug
Discontinued Application: 75256

Drug Name

DESOGESTREL AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

1999-08-12

75256 / 1

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

75256

Product Number

1

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

1999-08-12

Regulatory Status

Discontinued

1999
12 Aug
RX Application: 75256

Drug Name

DESOGESTREL AND ETHINYL ESTRADIOL

Product Number

2

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

1999-08-12

75256 / 2

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

75256

Product Number

2

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

1999-08-12

Regulatory Status

RX

-
Unclassified Application: 76455

Drug Name

DESOGESTREL; ETHINYL

Product Number

2

Dosage Form

-

Strength

0.125MG/0.025MG

Approval Date

-

76455 / 2

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

76455

Product Number

2

Dosage Form

-

Strength

0.125MG/0.025MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76455

Drug Name

DESOGESTREL; ETHINYL

Product Number

3

Dosage Form

-

Strength

0.15MG/0.025MG

Approval Date

-

76455 / 3

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

76455

Product Number

3

Dosage Form

-

Strength

0.15MG/0.025MG

Approval Date

-

Regulatory Status

Unclassified

1986
27 Aug
Discontinued Application: 70894

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-08-27

70894 / 1

Active Ingredient

DIAZEPAM

Application Number

70894

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-08-27

Regulatory Status

Discontinued

1986
27 Aug
Discontinued Application: 70895

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-08-27

70895 / 1

Active Ingredient

DIAZEPAM

Application Number

70895

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-08-27

Regulatory Status

Discontinued

1986
27 Aug
Discontinued Application: 70896

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-08-27

70896 / 1

Active Ingredient

DIAZEPAM

Application Number

70896

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-08-27

Regulatory Status

Discontinued

2001
16 Jul
Discontinued Application: 75809

Drug Name

ENPRESSE-21

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2001-07-16

75809 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75809

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2001-07-16

Regulatory Status

Discontinued

2001
16 Jul
RX Application: 75809

Drug Name

ENPRESSE-28

Product Number

2

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2001-07-16

75809 / 2

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

75809

Product Number

2

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2001-07-16

Regulatory Status

RX

1999
01 Nov
Discontinued Application: 40296

Drug Name

ESTROPIPATE

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1999-11-01

40296 / 1

Active Ingredient

ESTROPIPATE

Application Number

40296

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1999-11-01

Regulatory Status

Discontinued

1999
01 Nov
Discontinued Application: 40296

Drug Name

ESTROPIPATE

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

1999-11-01

40296 / 2

Active Ingredient

ESTROPIPATE

Application Number

40296

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

1999-11-01

Regulatory Status

Discontinued

1999
01 Nov
Discontinued Application: 40296

Drug Name

ESTROPIPATE

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

1999-11-01

40296 / 3

Active Ingredient

ESTROPIPATE

Application Number

40296

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

1999-11-01

Regulatory Status

Discontinued

1997
29 Dec
Discontinued Application: 40212

Drug Name

GYNODIOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1997-12-29

40212 / 1

Active Ingredient

ESTRADIOL

Application Number

40212

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1997-12-29

Regulatory Status

Discontinued

1997
29 Dec
Discontinued Application: 40212

Drug Name

GYNODIOL

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1997-12-29

40212 / 2

Active Ingredient

ESTRADIOL

Application Number

40212

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

1997-12-29

Regulatory Status

Discontinued

1997
29 Dec
Discontinued Application: 40212

Drug Name

GYNODIOL

Product Number

3

Dosage Form

-

Strength

1.5MG

Approval Date

1997-12-29

40212 / 3

Active Ingredient

ESTRADIOL

Application Number

40212

Product Number

3

Dosage Form

-

Strength

1.5MG

Approval Date

1997-12-29

Regulatory Status

Discontinued

1997
29 Dec
Discontinued Application: 40212

Drug Name

GYNODIOL

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

1997-12-29

40212 / 4

Active Ingredient

ESTRADIOL

Application Number

40212

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

1997-12-29

Regulatory Status

Discontinued

1986
04 Dec
Discontinued Application: 71216

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1986-12-04

71216 / 1

Active Ingredient

HALOPERIDOL

Application Number

71216

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1986-12-04

Regulatory Status

Discontinued

1986
04 Dec
Discontinued Application: 71217

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-12-04

71217 / 1

Active Ingredient

HALOPERIDOL

Application Number

71217

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-12-04

Regulatory Status

Discontinued

1986
04 Dec
Discontinued Application: 71218

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-04

71218 / 1

Active Ingredient

HALOPERIDOL

Application Number

71218

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-04

Regulatory Status

Discontinued

1986
04 Dec
Discontinued Application: 71219

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-12-04

71219 / 1

Active Ingredient

HALOPERIDOL

Application Number

71219

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-12-04

Regulatory Status

Discontinued

1987
07 Jul
Discontinued Application: 71220

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-07-07

71220 / 1

Active Ingredient

HALOPERIDOL

Application Number

71220

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-07-07

Regulatory Status

Discontinued

1987
07 Jul
Discontinued Application: 71221

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-07-07

71221 / 1

Active Ingredient

HALOPERIDOL

Application Number

71221

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-07-07

Regulatory Status

Discontinued

1984
29 Feb
Discontinued Application: 88593

Drug Name

HYDROXYZINE PAMOATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1984-02-29

88593 / 1

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

88593

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1984-02-29

Regulatory Status

Discontinued

1984
29 Feb
Discontinued Application: 88594

Drug Name

HYDROXYZINE PAMOATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1984-02-29

88594 / 1

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

88594

Product Number

1

Dosage Form

-

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1984-02-29

Regulatory Status

Discontinued

1984
29 Feb
Discontinued Application: 88595

Drug Name

HYDROXYZINE PAMOATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG HYDROCHLORIDE

Approval Date

1984-02-29

88595 / 1

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

88595

Product Number

1

Dosage Form

-

Strength

EQ 100MG HYDROCHLORIDE

Approval Date

1984-02-29

Regulatory Status

Discontinued

1985
18 Oct
Discontinued Application: 70326

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-10-18

70326 / 1

Active Ingredient

INDOMETHACIN

Application Number

70326

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1985-10-18

Regulatory Status

Discontinued

1985
18 Oct
Discontinued Application: 70327

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-10-18

70327 / 1

Active Ingredient

INDOMETHACIN

Application Number

70327

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-10-18

Regulatory Status

Discontinued

1983
17 Mar
Discontinued Application: 88119

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1983-03-17

88119 / 1

Active Ingredient

ISONIAZID

Application Number

88119

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1983-03-17

Regulatory Status

Discontinued

1983
17 Mar
Discontinued Application: 88231

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-03-17

88231 / 1

Active Ingredient

ISONIAZID

Application Number

88231

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-03-17

Regulatory Status

Discontinued

1997
29 Dec
Discontinued Application: 74991

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1997-12-29

74991 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

74991

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1997-12-29

Regulatory Status

Discontinued

1999
01 Dec
Discontinued Application: 40311

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1999-12-01

40311 / 1

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40311

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1999-12-01

Regulatory Status

Discontinued

1999
01 Dec
Discontinued Application: 40311

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1999-12-01

40311 / 2

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40311

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1999-12-01

Regulatory Status

Discontinued

1999
01 Dec
Discontinued Application: 40311

Drug Name

MEDROXYPROGESTERONE ACETATE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1999-12-01

40311 / 3

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

40311

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1999-12-01

Regulatory Status

Discontinued

1999
05 Oct
Discontinued Application: 40318

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1999-10-05

40318 / 1

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

40318

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1999-10-05

Regulatory Status

Discontinued

1999
05 Oct
Discontinued Application: 40318

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1999-10-05

40318 / 2

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

40318

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1999-10-05

Regulatory Status

Discontinued

1999
17 Jun
Discontinued Application: 40233

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1999-06-17

40233 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

40233

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1999-06-17

Regulatory Status

Discontinued

1986
16 Dec
Discontinued Application: 71006

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-12-16

71006 / 1

Active Ingredient

METHYLDOPA

Application Number

71006

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-12-16

Regulatory Status

Discontinued

1986
16 Dec
Discontinued Application: 71009

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-12-16

71009 / 1

Active Ingredient

METHYLDOPA

Application Number

71009

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-12-16

Regulatory Status

Discontinued

1984
21 Feb
Discontinued Application: 88497

Drug Name

METHYLPREDNISOLONE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1984-02-21

88497 / 1

Active Ingredient

METHYLPREDNISOLONE

Application Number

88497

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1984-02-21

Regulatory Status

Discontinued

1998
30 Jun
Discontinued Application: 40272

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

1998-06-30

40272 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40272

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

1998-06-30

Regulatory Status

Discontinued

1999
16 Mar
Discontinued Application: 40289

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1999-03-16

40289 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40289

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1999-03-16

Regulatory Status

Discontinued

1986
25 Apr
Discontinued Application: 88948

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1986-04-25

88948 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88948

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1986-04-25

Regulatory Status

Discontinued

1983
04 Oct
Discontinued Application: 88394

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-10-04

88394 / 1

Active Ingredient

PREDNISONE

Application Number

88394

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-10-04

Regulatory Status

Discontinued

1983
04 Oct
Discontinued Application: 88395

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-10-04

88395 / 1

Active Ingredient

PREDNISONE

Application Number

88395

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-10-04

Regulatory Status

Discontinued

1983
04 Oct
Discontinued Application: 88396

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-10-04

88396 / 1

Active Ingredient

PREDNISONE

Application Number

88396

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-10-04

Regulatory Status

Discontinued

1997
01 May
Discontinued Application: 40207

Drug Name

PROCHLORPERAZINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1997-05-01

40207 / 1

Active Ingredient

PROCHLORPERAZINE MALEATE

Application Number

40207

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1997-05-01

Regulatory Status

Discontinued

1997
01 May
Discontinued Application: 40207

Drug Name

PROCHLORPERAZINE MALEATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1997-05-01

40207 / 2

Active Ingredient

PROCHLORPERAZINE MALEATE

Application Number

40207

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1997-05-01

Regulatory Status

Discontinued

1987
20 Jan
Discontinued Application: 89484

Drug Name

PROCHLORPERAZINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-01-20

89484 / 1

Active Ingredient

PROCHLORPERAZINE MALEATE

Application Number

89484

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-01-20

Regulatory Status

Discontinued

1987
20 Jan
Discontinued Application: 89485

Drug Name

PROCHLORPERAZINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1987-01-20

89485 / 1

Active Ingredient

PROCHLORPERAZINE MALEATE

Application Number

89485

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1987-01-20

Regulatory Status

Discontinued

1987
20 Jan
Discontinued Application: 89486

Drug Name

PROCHLORPERAZINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-01-20

89486 / 1

Active Ingredient

PROCHLORPERAZINE MALEATE

Application Number

89486

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-01-20

Regulatory Status

Discontinued

1985
09 Sep
Discontinued Application: 70306

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-09-09

70306 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70306

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1985-09-09

Regulatory Status

Discontinued

1985
09 Sep
Discontinued Application: 70307

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1985-09-09

70307 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70307

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1985-09-09

Regulatory Status

Discontinued

1985
09 Sep
Discontinued Application: 70308

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1985-09-09

70308 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70308

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1985-09-09

Regulatory Status

Discontinued

1986
01 Oct
Discontinued Application: 70309

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-10-01

70309 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70309

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-10-01

Regulatory Status

Discontinued

1985
09 Sep
Discontinued Application: 70310

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1985-09-09

70310 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70310

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1985-09-09

Regulatory Status

Discontinued

1986
01 Oct
Discontinued Application: 71327

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

1986-10-01

71327 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

71327

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

1986-10-01

Regulatory Status

Discontinued

1987
02 Mar
Discontinued Application: 71126

Drug Name

PROPRANOLOL HYDROCHLORIDE & HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;40MG

Approval Date

1987-03-02

71126 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Application Number

71126

Product Number

1

Dosage Form

-

Strength

25MG;40MG

Approval Date

1987-03-02

Regulatory Status

Discontinued

1987
02 Mar
Discontinued Application: 71127

Drug Name

PROPRANOLOL HYDROCHLORIDE & HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;80MG

Approval Date

1987-03-02

71127 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Application Number

71127

Product Number

1

Dosage Form

-

Strength

25MG;80MG

Approval Date

1987-03-02

Regulatory Status

Discontinued

1988
29 Sep
Discontinued Application: 71708

Drug Name

TEMAZEPAM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-09-29

71708 / 1

Active Ingredient

TEMAZEPAM

Application Number

71708

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-09-29

Regulatory Status

Discontinued

1988
29 Sep
Discontinued Application: 71709

Drug Name

TEMAZEPAM

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1988-09-29

71709 / 1

Active Ingredient

TEMAZEPAM

Application Number

71709

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1988-09-29

Regulatory Status

Discontinued

1986
10 Jan
Discontinued Application: 70165

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-01-10

70165 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70165

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-01-10

Regulatory Status

Discontinued

1986
10 Jan
Discontinued Application: 70166

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-01-10

70166 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70166

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-01-10

Regulatory Status

Discontinued

1986
10 Jan
Discontinued Application: 70167

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-01-10

70167 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70167

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-01-10

Regulatory Status

Discontinued

1999
18 Jun
Discontinued Application: 75052

Drug Name

TRIAMTERENE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;37.5MG

Approval Date

1999-06-18

75052 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; TRIAMTERENE

Application Number

75052

Product Number

1

Dosage Form

-

Strength

25MG;37.5MG

Approval Date

1999-06-18

Regulatory Status

Discontinued

1985
23 Apr
Discontinued Application: 88967

Drug Name

TRIFLUOPERAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1985-04-23

88967 / 1

Active Ingredient

TRIFLUOPERAZINE HYDROCHLORIDE

Application Number

88967

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1985-04-23

Regulatory Status

Discontinued

1985
23 Apr
Discontinued Application: 88968

Drug Name

TRIFLUOPERAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1985-04-23

88968 / 1

Active Ingredient

TRIFLUOPERAZINE HYDROCHLORIDE

Application Number

88968

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1985-04-23

Regulatory Status

Discontinued

1985
23 Apr
Discontinued Application: 88969

Drug Name

TRIFLUOPERAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1985-04-23

88969 / 1

Active Ingredient

TRIFLUOPERAZINE HYDROCHLORIDE

Application Number

88969

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1985-04-23

Regulatory Status

Discontinued

1985
23 Apr
Discontinued Application: 88970

Drug Name

TRIFLUOPERAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-04-23

88970 / 1

Active Ingredient

TRIFLUOPERAZINE HYDROCHLORIDE

Application Number

88970

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-04-23

Regulatory Status

Discontinued

2004
24 Feb
RX Application: 76455

Drug Name

VELIVET

Product Number

1

Dosage Form

-

Strength

0.1MG,0.125MG,0.15MG;0.025MG,0.025MG,0.025MG

Approval Date

2004-02-24

76455 / 1

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

76455

Product Number

1

Dosage Form

-

Strength

0.1MG,0.125MG,0.15MG;0.025MG,0.025MG,0.025MG

Approval Date

2004-02-24

Regulatory Status

RX

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Drug Status Breakdown
86 total
  • Discontinued
  • RX
  • Unclassified
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

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

40223

Product Number

1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

-

Strength

300MG;15MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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