PUREPAC PHARM
FDA Approved Drugs

PUREPAC PHARM

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 162
  • Latest Approval Date Mar 31, 1997
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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Company

PUREPAC PHARM

Country

U.S.A

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Company Snapshot

PUREPAC PHARM

U.S.A

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FDA Approved Drug Records ( 162 records )
1982
01 Jan
Discontinued Application: 86681

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-01-01

86681 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

86681

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86683

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-01-01

86683 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

86683

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
17 Jul
Discontinued Application: 89080

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1986-07-17

89080 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

89080

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1986-07-17

Regulatory Status

Discontinued

1986
14 Apr
Discontinued Application: 70579

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-04-14

70579 / 1

Active Ingredient

ALLOPURINOL

Application Number

70579

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-04-14

Regulatory Status

Discontinued

1986
14 Apr
Discontinued Application: 70580

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1986-04-14

70580 / 1

Active Ingredient

ALLOPURINOL

Application Number

70580

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1986-04-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84699

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84699 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

84699

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85333

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

85333 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

85333

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88075

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-09-16

88075 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88075

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-09-16

Regulatory Status

Discontinued

1983
20 May
Discontinued Application: 88076

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-20

88076 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88076

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-20

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88077

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-09-16

88077 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88077

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-09-16

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88078

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1983-09-16

88078 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88078

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1983-09-16

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88079

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-09-16

88079 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88079

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-09-16

Regulatory Status

Discontinued

1983
18 Jul
Discontinued Application: 88084

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-07-18

88084 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88084

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-07-18

Regulatory Status

Discontinued

1983
18 Jul
Discontinued Application: 88085

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-07-18

88085 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88085

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-07-18

Regulatory Status

Discontinued

1983
18 Jul
Discontinued Application: 88105

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-07-18

88105 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88105

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-07-18

Regulatory Status

Discontinued

1983
18 Jul
Discontinued Application: 88106

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1983-07-18

88106 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88106

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1983-07-18

Regulatory Status

Discontinued

1983
18 Jul
Discontinued Application: 88107

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-07-18

88107 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88107

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1983-07-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61853

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61853 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61853

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61853

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61853 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61853

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61980

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61980 / 1

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61980

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61980

Drug Name

AMPICILLIN TRIHYDRATE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61980 / 2

Active Ingredient

AMPICILLIN/AMPICILLIN TRIHYDRATE

Application Number

61980

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997
31 Mar
Discontinued Application: 74640

Drug Name

CAPTOPRIL

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1997-03-31

74640 / 1

Active Ingredient

CAPTOPRIL

Application Number

74640

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1997-03-31

Regulatory Status

Discontinued

1997
31 Mar
Discontinued Application: 74640

Drug Name

CAPTOPRIL

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1997-03-31

74640 / 2

Active Ingredient

CAPTOPRIL

Application Number

74640

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1997-03-31

Regulatory Status

Discontinued

1997
31 Mar
Discontinued Application: 74640

Drug Name

CAPTOPRIL

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1997-03-31

74640 / 3

Active Ingredient

CAPTOPRIL

Application Number

74640

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1997-03-31

Regulatory Status

Discontinued

1997
31 Mar
Discontinued Application: 74640

Drug Name

CAPTOPRIL

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1997-03-31

74640 / 4

Active Ingredient

CAPTOPRIL

Application Number

74640

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1997-03-31

Regulatory Status

Discontinued

1989
05 Jan
Discontinued Application: 63017

Drug Name

CEFADROXIL

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-01-05

63017 / 1

Active Ingredient

CEFADROXIL/CEFADROXIL HEMIHYDRATE

Application Number

63017

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1989-01-05

Regulatory Status

Discontinued

1987
22 Apr
Discontinued Application: 62809

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-04-22

62809 / 1

Active Ingredient

CEPHALEXIN

Application Number

62809

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1987-04-22

Regulatory Status

Discontinued

1987
22 Apr
Discontinued Application: 62809

Drug Name

CEPHALEXIN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-22

62809 / 2

Active Ingredient

CEPHALEXIN

Application Number

62809

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1987-04-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84939

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84939 / 2

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84939

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85144

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85144 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85144

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85155

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

85155 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85155

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80886

Drug Name

CHLOROQUINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

80886 / 1

Active Ingredient

CHLOROQUINE PHOSPHATE

Application Number

80886

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86306

Drug Name

CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

86306 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

86306

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80403

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

80403 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80403

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80403

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

80403 / 2

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80403

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80403

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

80403 / 3

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80403

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80403

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80403 / 4

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80403

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80403

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

80403 / 5

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80403

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
16 Jul
Discontinued Application: 88139

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1986-07-16

88139 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

88139

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1986-07-16

Regulatory Status

Discontinued

1983
11 Aug
Discontinued Application: 88140

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-08-11

88140 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

88140

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-08-11

Regulatory Status

Discontinued

1988
25 Apr
Discontinued Application: 71924

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-04-25

71924 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71924

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1988
25 Apr
Discontinued Application: 71925

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-04-25

71925 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71925

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1988
25 Apr
Discontinued Application: 71926

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-04-25

71926 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71926

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1988
08 Aug
Discontinued Application: 72330

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-08-08

72330 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72330

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1988-08-08

Regulatory Status

Discontinued

1988
08 Aug
Discontinued Application: 72331

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-08-08

72331 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72331

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1988-08-08

Regulatory Status

Discontinued

1988
08 Aug
Discontinued Application: 72332

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-08-08

72332 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72332

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1988-08-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80493

Drug Name

CORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

80493 / 1

Active Ingredient

CORTISONE ACETATE

Application Number

80493

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84125

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84125 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

84125

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1996
07 May
Discontinued Application: 74285

Drug Name

DIFLUNISAL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1996-05-07

74285 / 1

Active Ingredient

DIFLUNISAL

Application Number

74285

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1996-05-07

Regulatory Status

Discontinued

1996
07 May
Discontinued Application: 74285

Drug Name

DIFLUNISAL

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1996-05-07

74285 / 2

Active Ingredient

DIFLUNISAL

Application Number

74285

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1996-05-07

Regulatory Status

Discontinued

1982
25 Jan
Discontinued Application: 83237

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-25

83237 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83237

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-25

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85150

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85150 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

85150

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85156

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85156 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

85156

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
12 Jul
Discontinued Application: 89425

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1990-07-12

89425 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

89425

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1990-07-12

Regulatory Status

Discontinued

1990
12 Jul
Discontinued Application: 89426

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-07-12

89426 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

89426

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-07-12

Regulatory Status

Discontinued

1990
12 Jul
Discontinued Application: 89427

Drug Name

DIPYRIDAMOLE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1990-07-12

89427 / 1

Active Ingredient

DIPYRIDAMOLE

Application Number

89427

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1990-07-12

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 72109

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1990-12-28

72109 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

72109

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1990-12-28

Regulatory Status

Discontinued

1988
08 Sep
Discontinued Application: 72110

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1988-09-08

72110 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

72110

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1988-09-08

Regulatory Status

Discontinued

1988
08 Sep
Discontinued Application: 72386

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1988-09-08

72386 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

72386

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1988-09-08

Regulatory Status

Discontinued

1988
08 Sep
Discontinued Application: 72387

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1988-09-08

72387 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

72387

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1988-09-08

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 73054

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1990-12-28

73054 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

73054

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1990-12-28

Regulatory Status

Discontinued

1990
28 Dec
Discontinued Application: 73055

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1990-12-28

73055 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

73055

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1990-12-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61743

Drug Name

ERYTHROMYCIN STEARATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61743 / 1

Active Ingredient

ERYTHROMYCIN STEARATE

Application Number

61743

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71551

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-09-09

71551 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

71551

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71927

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-09-09

71927 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

71927

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80784

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

80784 / 1

Active Ingredient

FOLIC ACID

Application Number

80784

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
29 Jan
Discontinued Application: 72929

Drug Name

GEMFIBROZIL

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1993-01-29

72929 / 1

Active Ingredient

GEMFIBROZIL

Application Number

72929

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1993-01-29

Regulatory Status

Discontinued

1994
31 Aug
Discontinued Application: 74360

Drug Name

GEMFIBROZIL

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1994-08-31

74360 / 1

Active Ingredient

GEMFIBROZIL

Application Number

74360

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1994-08-31

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 71071

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1986-11-03

71071 / 1

Active Ingredient

HALOPERIDOL

Application Number

71071

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 71072

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-11-03

71072 / 1

Active Ingredient

HALOPERIDOL

Application Number

71072

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 71073

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-11-03

71073 / 1

Active Ingredient

HALOPERIDOL

Application Number

71073

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 71074

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-11-03

71074 / 1

Active Ingredient

HALOPERIDOL

Application Number

71074

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1987
04 Aug
Discontinued Application: 71075

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-08-04

71075 / 1

Active Ingredient

HALOPERIDOL

Application Number

71075

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-08-04

Regulatory Status

Discontinued

1987
04 Aug
Discontinued Application: 71076

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-08-04

71076 / 1

Active Ingredient

HALOPERIDOL

Application Number

71076

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-08-04

Regulatory Status

Discontinued

1983
29 Jul
Discontinued Application: 88177

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-07-29

88177 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

88177

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-07-29

Regulatory Status

Discontinued

1983
15 Aug
Discontinued Application: 88178

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-08-15

88178 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

88178

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-08-15

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80395

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

80395 / 1

Active Ingredient

HYDROCORTISONE

Application Number

80395

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84247

Drug Name

HYDROCORTISONE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

84247 / 2

Active Ingredient

HYDROCORTISONE

Application Number

84247

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
31 Aug
Discontinued Application: 84247

Drug Name

HYDROCORTISONE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-08-31

84247 / 3

Active Ingredient

HYDROCORTISONE

Application Number

84247

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-08-31

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86050

Drug Name

HYDROCORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

86050 / 1

Active Ingredient

HYDROCORTISONE ACETATE

Application Number

86050

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86052

Drug Name

HYDROCORTISONE ACETATE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86052 / 1

Active Ingredient

HYDROCORTISONE ACETATE

Application Number

86052

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
25 Sep
Discontinued Application: 88120

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1984-09-25

88120 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88120

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984
25 Sep
Discontinued Application: 88121

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-09-25

88121 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88121

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984
25 Sep
Discontinued Application: 88122

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-09-25

88122 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88122

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1986
03 Oct
Discontinued Application: 71122

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1986-10-03

71122 / 1

Active Ingredient

IBUPROFEN

Application Number

71122

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1986-10-03

Regulatory Status

Discontinued

1986
19 Sep
Discontinued Application: 71123

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1986-09-19

71123 / 1

Active Ingredient

IBUPROFEN

Application Number

71123

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1986-09-19

Regulatory Status

Discontinued

1986
19 Sep
Discontinued Application: 71124

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1986-09-19

71124 / 1

Active Ingredient

IBUPROFEN

Application Number

71124

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1986-09-19

Regulatory Status

Discontinued

1986
19 Sep
Discontinued Application: 71125

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1986-09-19

71125 / 1

Active Ingredient

IBUPROFEN

Application Number

71125

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1986-09-19

Regulatory Status

Discontinued

1987
03 Feb
Discontinued Application: 71664

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-02-03

71664 / 1

Active Ingredient

IBUPROFEN

Application Number

71664

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-02-03

Regulatory Status

Discontinued

1988
01 Feb
Discontinued Application: 71964

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1988-02-01

71964 / 1

Active Ingredient

IBUPROFEN

Application Number

71964

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1988-02-01

Regulatory Status

Discontinued

1982
14 Jul
Discontinued Application: 80132

Drug Name

ISONIAZID

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-07-14

80132 / 3

Active Ingredient

ISONIAZID

Application Number

80132

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-07-14

Regulatory Status

Discontinued

1982
14 Jul
Discontinued Application: 80132

Drug Name

ISONIAZID

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1982-07-14

80132 / 4

Active Ingredient

ISONIAZID

Application Number

80132

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

1982-07-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84804

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84804 / 1

Active Ingredient

MEPROBAMATE

Application Number

84804

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84804

Drug Name

MEPROBAMATE

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

84804 / 2

Active Ingredient

MEPROBAMATE

Application Number

84804

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85718

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

85718 / 1

Active Ingredient

METHOCARBAMOL

Application Number

85718

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85718

Drug Name

METHOCARBAMOL

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

85718 / 2

Active Ingredient

METHOCARBAMOL

Application Number

85718

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
07 Feb
Discontinued Application: 70452

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-02-07

70452 / 1

Active Ingredient

METHYLDOPA

Application Number

70452

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-02-07

Regulatory Status

Discontinued

1986
07 Feb
Discontinued Application: 70749

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1986-02-07

70749 / 1

Active Ingredient

METHYLDOPA

Application Number

70749

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

1986-02-07

Regulatory Status

Discontinued

1986
07 Feb
Discontinued Application: 70750

Drug Name

METHYLDOPA

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-02-07

70750 / 1

Active Ingredient

METHYLDOPA

Application Number

70750

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-02-07

Regulatory Status

Discontinued

1986
24 Apr
Discontinued Application: 70688

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;250MG

Approval Date

1986-04-24

70688 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

70688

Product Number

1

Dosage Form

-

Strength

25MG;250MG

Approval Date

1986-04-24

Regulatory Status

Discontinued

1986
24 Apr
Discontinued Application: 70689

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG;500MG

Approval Date

1986-04-24

70689 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

70689

Product Number

1

Dosage Form

-

Strength

50MG;500MG

Approval Date

1986-04-24

Regulatory Status

Discontinued

1986
08 Oct
Discontinued Application: 70853

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

15MG;250MG

Approval Date

1986-10-08

70853 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

70853

Product Number

1

Dosage Form

-

Strength

15MG;250MG

Approval Date

1986-10-08

Regulatory Status

Discontinued

1986
08 Oct
Discontinued Application: 70854

Drug Name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

30MG;500MG

Approval Date

1986-10-08

70854 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; METHYLDOPA

Application Number

70854

Product Number

1

Dosage Form

-

Strength

30MG;500MG

Approval Date

1986-10-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80308

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80308 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

80308

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80309

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80309 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

80309

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80310

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

80310 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

80310

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80475

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80475 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

80475

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80475

Drug Name

METHYLTESTOSTERONE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80475 / 2

Active Ingredient

METHYLTESTOSTERONE

Application Number

80475

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80475

Drug Name

METHYLTESTOSTERONE

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

80475 / 3

Active Ingredient

METHYLTESTOSTERONE

Application Number

80475

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994
29 Jul
Discontinued Application: 74380

Drug Name

METOPROLOL TARTRATE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-07-29

74380 / 1

Active Ingredient

METOPROLOL TARTRATE

Application Number

74380

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1994-07-29

Regulatory Status

Discontinued

1994
29 Jul
Discontinued Application: 74380

Drug Name

METOPROLOL TARTRATE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-07-29

74380 / 2

Active Ingredient

METOPROLOL TARTRATE

Application Number

74380

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1994-07-29

Regulatory Status

Discontinued

1993
21 Dec
Discontinued Application: 74263

Drug Name

NAPROXEN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1993-12-21

74263 / 1

Active Ingredient

NAPROXEN

Application Number

74263

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993
21 Dec
Discontinued Application: 74263

Drug Name

NAPROXEN

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1993-12-21

74263 / 2

Active Ingredient

NAPROXEN

Application Number

74263

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1993
21 Dec
Discontinued Application: 74263

Drug Name

NAPROXEN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1993-12-21

74263 / 3

Active Ingredient

NAPROXEN

Application Number

74263

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1993-12-21

Regulatory Status

Discontinued

1995
20 Mar
Discontinued Application: 74319

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1995-03-20

74319 / 1

Active Ingredient

NAPROXEN SODIUM

Application Number

74319

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1995-03-20

Regulatory Status

Discontinued

1995
20 Mar
Discontinued Application: 74319

Drug Name

NAPROXEN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1995-03-20

74319 / 2

Active Ingredient

NAPROXEN SODIUM

Application Number

74319

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1995-03-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83271

Drug Name

NIACIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

83271 / 1

Active Ingredient

NIACIN

Application Number

83271

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60634

Drug Name

OXYTETRACYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

60634 / 1

Active Ingredient

OXYTETRACYCLINE HYDROCHLORIDE

Application Number

60634

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61588

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

61588 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

61588

Product Number

1

Dosage Form

-

Strength

200,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61588

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

61588 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

61588

Product Number

2

Dosage Form

-

Strength

250,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61588

Drug Name

PENICILLIN G POTASSIUM

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

61588 / 3

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

61588

Product Number

3

Dosage Form

-

Strength

400,000 UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61740

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

250,000 UNITS/5ML

Approval Date

1982-01-01

61740 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

61740

Product Number

1

Dosage Form

-

Strength

250,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61740

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

61740 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

61740

Product Number

2

Dosage Form

-

Strength

400,000 UNITS/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61571

Drug Name

PENICILLIN V POTASSIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE

Approval Date

1982-01-01

61571 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61571

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61571

Drug Name

PENICILLIN V POTASSIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

61571 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61571

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61571

Drug Name

PENICILLIN V POTASSIUM

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

61571 / 3

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61571

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61758

Drug Name

PENICILLIN V POTASSIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

61758 / 1

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61758

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61758

Drug Name

PENICILLIN V POTASSIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

61758 / 2

Active Ingredient

PENICILLIN V POTASSIUM

Application Number

61758

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
28 Apr
Discontinued Application: 74125

Drug Name

PINDOLOL

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-04-28

74125 / 1

Active Ingredient

PINDOLOL

Application Number

74125

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-04-28

Regulatory Status

Discontinued

1993
28 Apr
Discontinued Application: 74125

Drug Name

PINDOLOL

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1993-04-28

74125 / 2

Active Ingredient

PINDOLOL

Application Number

74125

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1993-04-28

Regulatory Status

Discontinued

1989
16 May
Discontinued Application: 72921

Drug Name

PRAZOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1989-05-16

72921 / 1

Active Ingredient

PRAZOSIN HYDROCHLORIDE

Application Number

72921

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1989-05-16

Regulatory Status

Discontinued

1989
16 May
Discontinued Application: 72991

Drug Name

PRAZOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1989-05-16

72991 / 1

Active Ingredient

PRAZOSIN HYDROCHLORIDE

Application Number

72991

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1989-05-16

Regulatory Status

Discontinued

1989
16 May
Discontinued Application: 72992

Drug Name

PRAZOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1989-05-16

72992 / 1

Active Ingredient

PRAZOSIN HYDROCHLORIDE

Application Number

72992

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1989-05-16

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80325

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80325 / 1

Active Ingredient

PREDNISOLONE

Application Number

80325

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80353

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80353 / 1

Active Ingredient

PREDNISONE

Application Number

80353

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86061

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

86061 / 1

Active Ingredient

PREDNISONE

Application Number

86061

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86062

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

86062 / 1

Active Ingredient

PREDNISONE

Application Number

86062

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83278

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

83278 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83278

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70757

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-11-03

70757 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70757

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70814

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-11-03

70814 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70814

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70815

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-11-03

70815 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70815

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70816

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-11-03

70816 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70816

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70817

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-11-03

70817 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70817

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84003

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84003 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

84003

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80842

Drug Name

RAUWOLFIA SERPENTINA

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

80842 / 1

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80842

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80842

Drug Name

RAUWOLFIA SERPENTINA

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

80842 / 2

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80842

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80753

Drug Name

RESERPINE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

80753 / 1

Active Ingredient

RESERPINE

Application Number

80753

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80753

Drug Name

RESERPINE

Product Number

2

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

80753 / 2

Active Ingredient

RESERPINE

Application Number

80753

Product Number

2

Dosage Form

-

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85867

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85867 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

85867

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83301

Drug Name

SODIUM PENTOBARBITAL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

83301 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

83301

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
14 Oct
Discontinued Application: 87998

Drug Name

SPIRONOLACTONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-10-14

87998 / 1

Active Ingredient

SPIRONOLACTONE

Application Number

87998

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-10-14

Regulatory Status

Discontinued

1983
25 Aug
Discontinued Application: 88053

Drug Name

SPIRONOLACTONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-08-25

88053 / 1

Active Ingredient

SPIRONOLACTONE

Application Number

88053

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-08-25

Regulatory Status

Discontinued

1985
06 Nov
Discontinued Application: 87999

Drug Name

SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1985-11-06

87999 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; SPIRONOLACTONE

Application Number

87999

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1985-11-06

Regulatory Status

Discontinued

1983
18 Aug
Discontinued Application: 88054

Drug Name

SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1983-08-18

88054 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; SPIRONOLACTONE

Application Number

88054

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1983-08-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80087

Drug Name

SULFISOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80087 / 1

Active Ingredient

SULFISOXAZOLE

Application Number

80087

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60290

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

60290 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60290

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60290

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

60290 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60290

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60291

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

60291 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

60291

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
17 Jun
Discontinued Application: 88950

Drug Name

TOLBUTAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1985-06-17

88950 / 1

Active Ingredient

TOLBUTAMIDE

Application Number

88950

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1985-06-17

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84020

Drug Name

TRIAMCINOLONE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

84020 / 2

Active Ingredient

TRIAMCINOLONE

Application Number

84020

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84020

Drug Name

TRIAMCINOLONE

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84020 / 3

Active Ingredient

TRIAMCINOLONE

Application Number

84020

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80086

Drug Name

TRIPLE SULFA

Product Number

1

Dosage Form

-

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

80086 / 1

Active Ingredient

TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)

Application Number

80086

Product Number

1

Dosage Form

-

Strength

167MG;167MG;167MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
162 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

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

86681

Product Number

1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

-

Strength

300MG;30MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

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