Par Pharmaceutical Discontinued
FDA Approved Drugs

Par Pharmaceutical 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 89
Latest Approval Date Oct 24, 2014
Data Source FDA
First Approval Date Jan 01, 1982

All

112

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Discontinued

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Company Overview

Company

Par Pharmaceutical Discontinued

Country

U.S.A

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Par Pharmaceutical Discontinued

300 Tice BoulevardWoodcliff Lake, NJ 07677

U.S.A

www.parpharm.com/ View on Map

FDA Approved Drug Records ( 89 records )

1984

25 Sep

Discontinued Application: 88697

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1984-09-25

88697 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88697

Product Number

Dosage Form

Strength

10MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984

25 Sep

Discontinued Application: 88698

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1984-09-25

88698 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88698

Product Number

Dosage Form

Strength

25MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984

25 Sep

Discontinued Application: 88699

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1984-09-25

88699 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88699

Product Number

Dosage Form

Strength

50MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984

25 Sep

Discontinued Application: 88700

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

75MG

Approval Date

1984-09-25

88700 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88700

Product Number

Dosage Form

Strength

75MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984

25 Sep

Discontinued Application: 88701

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-09-25

88701 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88701

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1984

25 Sep

Discontinued Application: 88702

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

150MG

Approval Date

1984-09-25

88702 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88702

Product Number

Dosage Form

Strength

150MG

Approval Date

1984-09-25

Regulatory Status

Discontinued

1997

04 Dec

Discontinued Application: 20696

Drug Name

ANTIZOL

Product Number

Dosage Form

Strength

1.5GM/1.5ML (1GM/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-12-04

20696 / 1 View Details

Active Ingredient

FOMEPIZOLE

Application Number

20696

Product Number

Dosage Form

Strength

1.5GM/1.5ML (1GM/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-12-04

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87009

Drug Name

BROMPHENIRAMINE MALEATE

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

87009 / 1 View Details

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

87009

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

27 Feb

Discontinued Application: 88175

Drug Name

CHLORPROPAMIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-02-27

88175 / 1 View Details

Active Ingredient

CHLORPROPAMIDE

Application Number

88175

Product Number

Dosage Form

Strength

100MG

Approval Date

1984-02-27

Regulatory Status

Discontinued

1984

27 Feb

Discontinued Application: 88176

Drug Name

CHLORPROPAMIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1984-02-27

88176 / 1 View Details

Active Ingredient

CHLORPROPAMIDE

Application Number

88176

Product Number

Dosage Form

Strength

250MG

Approval Date

1984-02-27

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70459

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

0.3MG

Approval Date

1986-07-08

70459 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70459

Product Number

Dosage Form

Strength

0.3MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70460

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

0.2MG

Approval Date

1986-07-08

70460 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70460

Product Number

Dosage Form

Strength

0.2MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1986

08 Jul

Discontinued Application: 70461

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1986-07-08

70461 / 1 View Details

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

70461

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1986-07-08

Regulatory Status

Discontinued

1987

16 Dec

Discontinued Application: 71142

Drug Name

CLONIDINE HYDROCHLORIDE AND CHLORTHALIDONE

Product Number

Dosage Form

Strength

15MG;0.3MG

Approval Date

1987-12-16

71142 / 1 View Details

Active Ingredient

CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Application Number

71142

Product Number

Dosage Form

Strength

15MG;0.3MG

Approval Date

1987-12-16

Regulatory Status

Discontinued

1987

16 Dec

Discontinued Application: 71178

Drug Name

CLONIDINE HYDROCHLORIDE AND CHLORTHALIDONE

Product Number

Dosage Form

Strength

15MG;0.2MG

Approval Date

1987-12-16

71178 / 1 View Details

Active Ingredient

CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Application Number

71178

Product Number

Dosage Form

Strength

15MG;0.2MG

Approval Date

1987-12-16

Regulatory Status

Discontinued

1987

16 Dec

Discontinued Application: 71179

Drug Name

CLONIDINE HYDROCHLORIDE AND CHLORTHALIDONE

Product Number

Dosage Form

Strength

15MG;0.1MG

Approval Date

1987-12-16

71179 / 1 View Details

Active Ingredient

CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Application Number

71179

Product Number

Dosage Form

Strength

15MG;0.1MG

Approval Date

1987-12-16

Regulatory Status

Discontinued

2005

26 Apr

Discontinued Application: 75162

Drug Name

CLOZAPINE

Product Number

Dosage Form

Strength

25MG

Approval Date

2005-04-26

75162 / 1 View Details

Active Ingredient

CLOZAPINE

Application Number

75162

Product Number

Dosage Form

Strength

25MG

Approval Date

2005-04-26

Regulatory Status

Discontinued

2005

26 Apr

Discontinued Application: 75162

Drug Name

CLOZAPINE

Product Number

Dosage Form

Strength

100MG

Approval Date

2005-04-26

75162 / 2 View Details

Active Ingredient

CLOZAPINE

Application Number

75162

Product Number

Dosage Form

Strength

100MG

Approval Date

2005-04-26

Regulatory Status

Discontinued

1987

02 Jul

Discontinued Application: 70156

Drug Name

DOXY-SLEEP-AID

Product Number

Dosage Form

Strength

25MG

Approval Date

1987-07-02

70156 / 1 View Details

Active Ingredient

DOXYLAMINE SUCCINATE

Application Number

70156

Product Number

Dosage Form

Strength

25MG

Approval Date

1987-07-02

Regulatory Status

Discontinued

1984

19 Oct

Discontinued Application: 62434

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1984-10-19

62434 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62434

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1984-10-19

Regulatory Status

Discontinued

1983

22 Dec

Discontinued Application: 62442

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1983-12-22

62442 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62442

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1983-12-22

Regulatory Status

Discontinued

1988

22 Aug

Discontinued Application: 72437

Drug Name

FENOPROFEN CALCIUM

Product Number

Dosage Form

Strength

EQ 200MG BASE

Approval Date

1988-08-22

72437 / 1 View Details

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72437

Product Number

Dosage Form

Strength

EQ 200MG BASE

Approval Date

1988-08-22

Regulatory Status

Discontinued

1988

22 Aug

Discontinued Application: 72438

Drug Name

FENOPROFEN CALCIUM

Product Number

Dosage Form

Strength

EQ 300MG BASE

Approval Date

1988-08-22

72438 / 1 View Details

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72438

Product Number

Dosage Form

Strength

EQ 300MG BASE

Approval Date

1988-08-22

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 0.2MG BASE

Approval Date

2009-10-30

77312 / 1 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 0.2MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 0.4MG BASE

Approval Date

2009-10-30

77312 / 2 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 0.4MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 0.6MG BASE

Approval Date

2009-10-30

77312 / 3 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 0.6MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 0.8MG BASE

Approval Date

2009-10-30

77312 / 4 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 0.8MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 1.2MG BASE

Approval Date

2009-10-30

77312 / 5 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 1.2MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009

30 Oct

Discontinued Application: 77312

Drug Name

FENTANYL CITRATE

Product Number

Dosage Form

Strength

EQ 1.6MG BASE

Approval Date

2009-10-30

77312 / 6 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

77312

Product Number

Dosage Form

Strength

EQ 1.6MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

1987

20 Jul

Discontinued Application: 71328

Drug Name

HALOPERIDOL

Product Number

Dosage Form

Strength

20MG

Approval Date

1987-07-20

71328 / 1 View Details

Active Ingredient

HALOPERIDOL

Application Number

71328

Product Number

Dosage Form

Strength

20MG

Approval Date

1987-07-20

Regulatory Status

Discontinued

1990

25 Dec

Discontinued Application: 70347

Drug Name

HYDRO-RIDE

Product Number

Dosage Form

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1990-12-25

70347 / 1 View Details

Active Ingredient

AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

70347

Product Number

Dosage Form

Strength

EQ 5MG ANHYDROUS;50MG

Approval Date

1990-12-25

Regulatory Status

Discontinued

1985

31 May

Discontinued Application: 88850

Drug Name

HYDROFLUMETHIAZIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1985-05-31

88850 / 1 View Details

Active Ingredient

HYDROFLUMETHIAZIDE

Application Number

88850

Product Number

Dosage Form

Strength

50MG

Approval Date

1985-05-31

Regulatory Status

Discontinued

1982

11 Jun

Discontinued Application: 87656

Drug Name

HYDROXYZINE PAMOATE

Product Number

Dosage Form

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1982-06-11

87656 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

87656

Product Number

Dosage Form

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1982-06-11

Regulatory Status

Discontinued

1982

11 Jun

Discontinued Application: 87657

Drug Name

HYDROXYZINE PAMOATE

Product Number

Dosage Form

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1982-06-11

87657 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

87657

Product Number

Dosage Form

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1982-06-11

Regulatory Status

Discontinued

1982

11 Jun

Discontinued Application: 87658

Drug Name

HYDROXYZINE PAMOATE

Product Number

Dosage Form

Strength

EQ 100MG HYDROCHLORIDE

Approval Date

1982-06-11

87658 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

87658

Product Number

Dosage Form

Strength

EQ 100MG HYDROCHLORIDE

Approval Date

1982-06-11

Regulatory Status

Discontinued

1986

17 Mar

Discontinued Application: 89145

Drug Name

HYDROXYZINE PAMOATE

Product Number

Dosage Form

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1986-03-17

89145 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

89145

Product Number

Dosage Form

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1986-03-17

Regulatory Status

Discontinued

1986

17 Mar

Discontinued Application: 89146

Drug Name

HYDROXYZINE PAMOATE

Product Number

Dosage Form

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1986-03-17

89146 / 1 View Details

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

89146

Product Number

Dosage Form

Strength

EQ 50MG HYDROCHLORIDE

Approval Date

1986-03-17

Regulatory Status

Discontinued

1985

06 Aug

Discontinued Application: 70328

Drug Name

IBUPROFEN

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-08-06

70328 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

70328

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-08-06

Regulatory Status

Discontinued

1987

14 Jul

Discontinued Application: 89422

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1987-07-14

89422 / 1 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

89422

Product Number

Dosage Form

Strength

10MG

Approval Date

1987-07-14

Regulatory Status

Discontinued

1987

14 Jul

Discontinued Application: 89497

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1987-07-14

89497 / 1 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

89497

Product Number

Dosage Form

Strength

25MG

Approval Date

1987-07-14

Regulatory Status

Discontinued

1987

14 Oct

Discontinued Application: 71598

Drug Name

LEUCOVORIN CALCIUM

Product Number

Dosage Form

Strength

EQ 25MG BASE

Approval Date

1987-10-14

71598 / 1 View Details

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

71598

Product Number

Dosage Form

Strength

EQ 25MG BASE

Approval Date

1987-10-14

Regulatory Status

Discontinued

1987

14 Oct

Discontinued Application: 71600

Drug Name

LEUCOVORIN CALCIUM

Product Number

Dosage Form

Strength

EQ 5MG BASE

Approval Date

1987-10-14

71600 / 1 View Details

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

71600

Product Number

Dosage Form

Strength

EQ 5MG BASE

Approval Date

1987-10-14

Regulatory Status

Discontinued

1986

01 Dec

Discontinued Application: 70675

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1986-12-01

70675 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70675

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1986-12-01

Regulatory Status

Discontinued

1986

01 Dec

Discontinued Application: 70676

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

1MG

Approval Date

1986-12-01

70676 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70676

Product Number

Dosage Form

Strength

1MG

Approval Date

1986-12-01

Regulatory Status

Discontinued

1986

01 Dec

Discontinued Application: 70677

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

2MG

Approval Date

1986-12-01

70677 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70677

Product Number

Dosage Form

Strength

2MG

Approval Date

1986-12-01

Regulatory Status

Discontinued

1988

10 Mar

Discontinued Application: 72077

Drug Name

MECLOFENAMATE SODIUM

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1988-03-10

72077 / 1 View Details

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

72077

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1988-03-10

Regulatory Status

Discontinued

1988

10 Mar

Discontinued Application: 72078

Drug Name

MECLOFENAMATE SODIUM

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1988-03-10

72078 / 1 View Details

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

72078

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1988-03-10

Regulatory Status

Discontinued

1986

19 Aug

Discontinued Application: 89126

Drug Name

MEPROBAMATE AND ASPIRIN

Product Number

Dosage Form

Strength

325MG;200MG

Approval Date

1986-08-19

89126 / 1 View Details

Active Ingredient

ASPIRIN; MEPROBAMATE

Application Number

89126

Product Number

Dosage Form

Strength

325MG;200MG

Approval Date

1986-08-19

Regulatory Status

Discontinued

1988

04 Nov

Discontinued Application: 89657

Drug Name

METHOCARBAMOL AND ASPIRIN

Product Number

Dosage Form

Strength

325MG;400MG

Approval Date

1988-11-04

89657 / 1 View Details

Active Ingredient

ASPIRIN; METHOCARBAMOL

Application Number

89657

Product Number

Dosage Form

Strength

325MG;400MG

Approval Date

1988-11-04

Regulatory Status

Discontinued

1986

12 Feb

Discontinued Application: 89135

Drug Name

METHYCLOTHIAZIDE

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1986-02-12

89135 / 1 View Details

Active Ingredient

METHYCLOTHIAZIDE

Application Number

89135

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1986-02-12

Regulatory Status

Discontinued

1986

12 Feb

Discontinued Application: 89136

Drug Name

METHYCLOTHIAZIDE

Product Number

Dosage Form

Strength

5MG

Approval Date

1986-02-12

89136 / 1 View Details

Active Ingredient

METHYCLOTHIAZIDE

Application Number

89136

Product Number

Dosage Form

Strength

5MG

Approval Date

1986-02-12

Regulatory Status

Discontinued

1987

06 Nov

Discontinued Application: 70654

Drug Name

METHYLDOPA AND CHLOROTHIAZIDE

Product Number

Dosage Form

Strength

250MG;250MG

Approval Date

1987-11-06

70654 / 1 View Details

Active Ingredient

CHLOROTHIAZIDE; METHYLDOPA

Application Number

70654

Product Number

Dosage Form

Strength

250MG;250MG

Approval Date

1987-11-06

Regulatory Status

Discontinued

1987

06 Nov

Discontinued Application: 70783

Drug Name

METHYLDOPA AND CHLOROTHIAZIDE

Product Number

Dosage Form

Strength

150MG;250MG

Approval Date

1987-11-06

70783 / 1 View Details

Active Ingredient

CHLOROTHIAZIDE; METHYLDOPA

Application Number

70783

Product Number

Dosage Form

Strength

150MG;250MG

Approval Date

1987-11-06

Regulatory Status

Discontinued

1988

25 Apr

Discontinued Application: 89207

Drug Name

METHYLPREDNISOLONE

Product Number

Dosage Form

Strength

16MG

Approval Date

1988-04-25

89207 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE

Application Number

89207

Product Number

Dosage Form

Strength

16MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1988

25 Apr

Discontinued Application: 89208

Drug Name

METHYLPREDNISOLONE

Product Number

Dosage Form

Strength

24MG

Approval Date

1988-04-25

89208 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE

Application Number

89208

Product Number

Dosage Form

Strength

24MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1988

25 Apr

Discontinued Application: 89209

Drug Name

METHYLPREDNISOLONE

Product Number

Dosage Form

Strength

32MG

Approval Date

1988-04-25

89209 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE

Application Number

89209

Product Number

Dosage Form

Strength

32MG

Approval Date

1988-04-25

Regulatory Status

Discontinued

1986

25 Mar

Discontinued Application: 70342

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

1986-03-25

70342 / 1 View Details

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

70342

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

1986-03-25

Regulatory Status

Discontinued

2007

22 Jun

Discontinued Application: 77827

Drug Name

OXANDROLONE

Product Number

Dosage Form

Strength

2.5MG

Approval Date

2007-06-22

77827 / 1 View Details

Active Ingredient

OXANDROLONE

Application Number

77827

Product Number

Dosage Form

Strength

2.5MG

Approval Date

2007-06-22

Regulatory Status

Discontinued

2007

22 Jun

Discontinued Application: 77827

Drug Name

OXANDROLONE

Product Number

Dosage Form

Strength

10MG

Approval Date

2007-06-22

77827 / 2 View Details

Active Ingredient

OXANDROLONE

Application Number

77827

Product Number

Dosage Form

Strength

10MG

Approval Date

2007-06-22

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

5MG

Approval Date

2014-10-24

200792 / 1 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

5MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

7.5MG

Approval Date

2014-10-24

200792 / 2 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

7.5MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

2014-10-24

200792 / 3 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

10MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

15MG

Approval Date

2014-10-24

200792 / 4 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

15MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

20MG

Approval Date

2014-10-24

200792 / 5 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

20MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

30MG

Approval Date

2014-10-24

200792 / 6 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

30MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

2014

24 Oct

Discontinued Application: 200792

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

40MG

Approval Date

2014-10-24

200792 / 7 View Details

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

200792

Product Number

Dosage Form

Strength

40MG

Approval Date

2014-10-24

Regulatory Status

Discontinued

1986

11 Sep

Discontinued Application: 70565

Drug Name

PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG;2MG

Approval Date

1986-09-11

70565 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

70565

Product Number

Dosage Form

Strength

10MG;2MG

Approval Date

1986-09-11

Regulatory Status

Discontinued

1986

11 Sep

Discontinued Application: 70574

Drug Name

PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG;4MG

Approval Date

1986-09-11

70574 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

70574

Product Number

Dosage Form

Strength

50MG;4MG

Approval Date

1986-09-11

Regulatory Status

Discontinued

1986

11 Sep

Discontinued Application: 70595

Drug Name

PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG;4MG

Approval Date

1986-09-11

70595 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

70595

Product Number

Dosage Form

Strength

25MG;4MG

Approval Date

1986-09-11

Regulatory Status

Discontinued

1986

11 Sep

Discontinued Application: 70620

Drug Name

PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG;4MG

Approval Date

1986-09-11

70620 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

70620

Product Number

Dosage Form

Strength

10MG;4MG

Approval Date

1986-09-11

Regulatory Status

Discontinued

1986

11 Sep

Discontinued Application: 70621

Drug Name

PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG;2MG

Approval Date

1986-09-11

70621 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

70621

Product Number

Dosage Form

Strength

25MG;2MG

Approval Date

1986-09-11

Regulatory Status

Discontinued

1983

08 Dec

Discontinued Application: 88377

Drug Name

PROPANTHELINE BROMIDE

Product Number

Dosage Form

Strength

15MG

Approval Date

1983-12-08

88377 / 1 View Details

Active Ingredient

PROPANTHELINE BROMIDE

Application Number

88377

Product Number

Dosage Form

Strength

15MG

Approval Date

1983-12-08

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80269

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

80269 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

80269

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

20 Sep

Discontinued Application: 88907

Drug Name

RESERPINE AND HYDROFLUMETHIAZIDE

Product Number

Dosage Form

Strength

50MG;0.125MG

Approval Date

1985-09-20

88907 / 1 View Details

Active Ingredient

HYDROFLUMETHIAZIDE; RESERPINE

Application Number

88907

Product Number

Dosage Form

Strength

50MG;0.125MG

Approval Date

1985-09-20

Regulatory Status

Discontinued

1985

06 Sep

Discontinued Application: 88933

Drug Name

SULFINPYRAZONE

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-09-06

88933 / 1 View Details

Active Ingredient

SULFINPYRAZONE

Application Number

88933

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-09-06

Regulatory Status

Discontinued

1985

06 Sep

Discontinued Application: 88934

Drug Name

SULFINPYRAZONE

Product Number

Dosage Form

Strength

200MG

Approval Date

1985-09-06

88934 / 1 View Details

Active Ingredient

SULFINPYRAZONE

Application Number

88934

Product Number

Dosage Form

Strength

200MG

Approval Date

1985-09-06

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88322

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-12-05

88322 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88322

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-12-05

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88336

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-12-05

88336 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88336

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-12-05

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88351

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-12-05

88351 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88351

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-12-05

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88352

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

15MG

Approval Date

1983-12-05

88352 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88352

Product Number

Dosage Form

Strength

15MG

Approval Date

1983-12-05

Regulatory Status

Discontinued

1983

29 Dec

Discontinued Application: 88480

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1983-12-29

88480 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88480

Product Number

Dosage Form

Strength

100MG

Approval Date

1983-12-29

Regulatory Status

Discontinued

1988

09 Feb

Discontinued Application: 89764

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

150MG

Approval Date

1988-02-09

89764 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

89764

Product Number

Dosage Form

Strength

150MG

Approval Date

1988-02-09

Regulatory Status

Discontinued

1988

09 Feb

Discontinued Application: 89765

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

200MG

Approval Date

1988-02-09

89765 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

89765

Product Number

Dosage Form

Strength

200MG

Approval Date

1988-02-09

Regulatory Status

Discontinued

1986

06 Jan

Discontinued Application: 70159

Drug Name

TOLAZAMIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1986-01-06

70159 / 1 View Details

Active Ingredient

TOLAZAMIDE

Application Number

70159

Product Number

Dosage Form

Strength

100MG

Approval Date

1986-01-06

Regulatory Status

Discontinued

1986

06 Jan

Discontinued Application: 70160

Drug Name

TOLAZAMIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-01-06

70160 / 1 View Details

Active Ingredient

TOLAZAMIDE

Application Number

70160

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-01-06

Regulatory Status

Discontinued

1986

06 Jan

Discontinued Application: 70161

Drug Name

TOLAZAMIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1986-01-06

70161 / 1 View Details

Active Ingredient

TOLAZAMIDE

Application Number

70161

Product Number

Dosage Form

Strength

500MG

Approval Date

1986-01-06

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87005

Drug Name

TRICHLORMETHIAZIDE

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

87005 / 1 View Details

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

87005

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87007

Drug Name

TRICHLORMETHIAZIDE

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

87007 / 1 View Details

Active Ingredient

TRICHLORMETHIAZIDE

Application Number

87007

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

28 Feb

Discontinued Application: 70431

Drug Name

VALPROIC ACID

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-02-28

70431 / 1 View Details

Active Ingredient

VALPROIC ACID

Application Number

70431

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-02-28

Regulatory Status

Discontinued

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Discontinued

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Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Application Number

88697

Product Number

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Dosage Form

Strength

10MG

FDA Approved Drug Data

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