Mutual Pharmaceutical Company, Inc. Discontinued
FDA Approved Drugs

Mutual Pharmaceutical Company, Inc. 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 58
Latest Approval Date Jan 22, 1998
Data Source FDA
First Approval Date Jan 01, 1982

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Company Overview

Company

Mutual Pharmaceutical Company, Inc. Discontinued

Country

U.S.A

Website

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Company Snapshot

Mutual Pharmaceutical Company, Inc. Discontinued

1100 Orthodox StreetPhiladelphia, PA, 19137

U.S.A

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FDA Approved Drug Records ( 58 records )

1982

01 Jan

Discontinued Application: 85794

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

Dosage Form

Strength

300MG;30MG

Approval Date

1982-01-01

85794 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

85794

Product Number

Dosage Form

Strength

300MG;30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85795

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

Dosage Form

Strength

300MG;15MG

Approval Date

1982-01-01

85795 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

85795

Product Number

Dosage Form

Strength

300MG;15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

13 Apr

Discontinued Application: 87653

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

Dosage Form

Strength

300MG;60MG

Approval Date

1982-04-13

87653 / 1 View Details

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

87653

Product Number

Dosage Form

Strength

300MG;60MG

Approval Date

1982-04-13

Regulatory Status

Discontinued

1985

24 Dec

Discontinued Application: 70466

Drug Name

ALLOPURINOL

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-12-24

70466 / 1 View Details

Active Ingredient

ALLOPURINOL

Application Number

70466

Product Number

Dosage Form

Strength

100MG

Approval Date

1985-12-24

Regulatory Status

Discontinued

1985

24 Dec

Discontinued Application: 70467

Drug Name

ALLOPURINOL

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-12-24

70467 / 1 View Details

Active Ingredient

ALLOPURINOL

Application Number

70467

Product Number

Dosage Form

Strength

300MG

Approval Date

1985-12-24

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85627

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

85627 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85627

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

11 May

Discontinued Application: 85742

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-05-11

85742 / 2 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85742

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-05-11

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85743

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

75MG

Approval Date

1982-01-01

85743 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85743

Product Number

Dosage Form

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85744

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

85744 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85744

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85745

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

85745 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

85745

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

17 Feb

Discontinued Application: 89423

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

150MG

Approval Date

1987-02-17

89423 / 1 View Details

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

89423

Product Number

Dosage Form

Strength

150MG

Approval Date

1987-02-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87292

Drug Name

CHLORTHALIDONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

87292 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

87292

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87293

Drug Name

CHLORTHALIDONE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

87293 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

87293

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

19 Sep

Discontinued Application: 89738

Drug Name

CHLORTHALIDONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1988-09-19

89738 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

89738

Product Number

Dosage Form

Strength

25MG

Approval Date

1988-09-19

Regulatory Status

Discontinued

1988

19 Sep

Discontinued Application: 89739

Drug Name

CHLORTHALIDONE

Product Number

Dosage Form

Strength

50MG

Approval Date

1988-09-19

89739 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

89739

Product Number

Dosage Form

Strength

50MG

Approval Date

1988-09-19

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84506

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

84506 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

84506

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

30 Sep

Discontinued Application: 62391

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1982-09-30

62391 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62391

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1982-09-30

Regulatory Status

Discontinued

1983

28 Jan

Discontinued Application: 62418

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1983-01-28

62418 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62418

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1983-01-28

Regulatory Status

Discontinued

1983

28 Jan

Discontinued Application: 62418

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1983-01-28

62418 / 2 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62418

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1983-01-28

Regulatory Status

Discontinued

1985

01 Nov

Discontinued Application: 88891

Drug Name

ERGOLOID MESYLATES

Product Number

Dosage Form

Strength

1MG

Approval Date

1985-11-01

88891 / 1 View Details

Active Ingredient

ERGOLOID MESYLATES

Application Number

88891

Product Number

Dosage Form

Strength

1MG

Approval Date

1985-11-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84106

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

84106 / 2 View Details

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

84106

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84107

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

84107 / 2 View Details

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

84107

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

11 Apr

Discontinued Application: 88728

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1985-04-11

88728 / 1 View Details

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

88728

Product Number

Dosage Form

Strength

10MG

Approval Date

1985-04-11

Regulatory Status

Discontinued

1997

25 Sep

Discontinued Application: 40236

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1997-09-25

40236 / 1 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40236

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1997-09-25

Regulatory Status

Discontinued

1997

25 Sep

Discontinued Application: 40236

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

750MG;7.5MG

Approval Date

1997-09-25

40236 / 2 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40236

Product Number

Dosage Form

Strength

750MG;7.5MG

Approval Date

1997-09-25

Regulatory Status

Discontinued

1997

26 Nov

Discontinued Application: 40240

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;10MG

Approval Date

1997-11-26

40240 / 1 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40240

Product Number

Dosage Form

Strength

650MG;10MG

Approval Date

1997-11-26

Regulatory Status

Discontinued

1997

26 Nov

Discontinued Application: 40240

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;7.5MG

Approval Date

1997-11-26

40240 / 2 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40240

Product Number

Dosage Form

Strength

650MG;7.5MG

Approval Date

1997-11-26

Regulatory Status

Discontinued

1983

18 Apr

Discontinued Application: 87857

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-04-18

87857 / 1 View Details

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

87857

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-04-18

Regulatory Status

Discontinued

1983

18 Apr

Discontinued Application: 87860

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-04-18

87860 / 1 View Details

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

87860

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-04-18

Regulatory Status

Discontinued

1983

15 Nov

Discontinued Application: 88409

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-11-15

88409 / 1 View Details

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88409

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-11-15

Regulatory Status

Discontinued

1986

03 Oct

Discontinued Application: 70067

Drug Name

INDOMETHACIN

Product Number

Dosage Form

Strength

25MG

Approval Date

1986-10-03

70067 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

70067

Product Number

Dosage Form

Strength

25MG

Approval Date

1986-10-03

Regulatory Status

Discontinued

1986

03 Oct

Discontinued Application: 70068

Drug Name

INDOMETHACIN

Product Number

Dosage Form

Strength

50MG

Approval Date

1986-10-03

70068 / 1 View Details

Active Ingredient

INDOMETHACIN

Application Number

70068

Product Number

Dosage Form

Strength

50MG

Approval Date

1986-10-03

Regulatory Status

Discontinued

1985

10 Dec

Discontinued Application: 70472

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1985-12-10

70472 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70472

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1985-12-10

Regulatory Status

Discontinued

1985

10 Dec

Discontinued Application: 70473

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

1MG

Approval Date

1985-12-10

70473 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70473

Product Number

Dosage Form

Strength

1MG

Approval Date

1985-12-10

Regulatory Status

Discontinued

1985

10 Dec

Discontinued Application: 70474

Drug Name

LORAZEPAM

Product Number

Dosage Form

Strength

2MG

Approval Date

1985-12-10

70474 / 1 View Details

Active Ingredient

LORAZEPAM

Application Number

70474

Product Number

Dosage Form

Strength

2MG

Approval Date

1985-12-10

Regulatory Status

Discontinued

1987

10 Feb

Discontinued Application: 70660

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

1987-02-10

70660 / 1 View Details

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

70660

Product Number

Dosage Form

Strength

EQ 10MG BASE

Approval Date

1987-02-10

Regulatory Status

Discontinued

1983

16 Feb

Discontinued Application: 18818

Drug Name

METRONIDAZOLE

Product Number

Dosage Form

Strength

250MG

Approval Date

1983-02-16

18818 / 1 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18818

Product Number

Dosage Form

Strength

250MG

Approval Date

1983-02-16

Regulatory Status

Discontinued

1983

16 Feb

Discontinued Application: 18818

Drug Name

METRONIDAZOLE

Product Number

Dosage Form

Strength

500MG

Approval Date

1983-02-16

18818 / 2 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18818

Product Number

Dosage Form

Strength

500MG

Approval Date

1983-02-16

Regulatory Status

Discontinued

1998

22 Jan

Discontinued Application: 40219

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1998-01-22

40219 / 1 View Details

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40219

Product Number

Dosage Form

Strength

500MG;5MG

Approval Date

1998-01-22

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80701

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

80701 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

80701

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84634

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

84634 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

84634

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86595

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

86595 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

86595

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83186

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

83186 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83186

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

12 Jun

Discontinued Application: 70115

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

325MG;50MG

Approval Date

1985-06-12

70115 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70115

Product Number

Dosage Form

Strength

325MG;50MG

Approval Date

1985-06-12

Regulatory Status

Discontinued

1985

12 Jun

Discontinued Application: 70116

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1985-06-12

70116 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70116

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1985-06-12

Regulatory Status

Discontinued

1986

21 Mar

Discontinued Application: 70615

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

70615 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70615

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

Regulatory Status

Discontinued

1986

21 Mar

Discontinued Application: 70771

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

70771 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70771

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

Regulatory Status

Discontinued

1986

21 Mar

Discontinued Application: 70775

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

70775 / 1 View Details

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

70775

Product Number

Dosage Form

Strength

650MG;100MG

Approval Date

1986-03-21

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87265

Drug Name

SPIRONOLACTONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

87265 / 1 View Details

Active Ingredient

SPIRONOLACTONE

Application Number

87265

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87267

Drug Name

SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

25MG;25MG

Approval Date

1982-01-01

87267 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE; SPIRONOLACTONE

Application Number

87267

Product Number

Dosage Form

Strength

25MG;25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

14 Nov

Discontinued Application: 70006

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

Dosage Form

Strength

400MG;80MG

Approval Date

1984-11-14

70006 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70006

Product Number

Dosage Form

Strength

400MG;80MG

Approval Date

1984-11-14

Regulatory Status

Discontinued

1984

14 Nov

Discontinued Application: 70007

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM DOUBLE STRENGTH

Product Number

Dosage Form

Strength

800MG;160MG

Approval Date

1984-11-14

70007 / 1 View Details

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70007

Product Number

Dosage Form

Strength

800MG;160MG

Approval Date

1984-11-14

Regulatory Status

Discontinued

1983

18 Nov

Discontinued Application: 87264

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-11-18

87264 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

87264

Product Number

Dosage Form

Strength

25MG

Approval Date

1983-11-18

Regulatory Status

Discontinued

1983

18 Nov

Discontinued Application: 88370

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-11-18

88370 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88370

Product Number

Dosage Form

Strength

50MG

Approval Date

1983-11-18

Regulatory Status

Discontinued

1983

18 Nov

Discontinued Application: 88375

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-11-18

88375 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88375

Product Number

Dosage Form

Strength

10MG

Approval Date

1983-11-18

Regulatory Status

Discontinued

1983

16 Nov

Discontinued Application: 88379

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

100MG

Approval Date

1983-11-16

88379 / 1 View Details

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88379

Product Number

Dosage Form

Strength

100MG

Approval Date

1983-11-16

Regulatory Status

Discontinued

1986

24 Sep

Discontinued Application: 70482

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

Dosage Form

Strength

80MG

Approval Date

1986-09-24

70482 / 1 View Details

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70482

Product Number

Dosage Form

Strength

80MG

Approval Date

1986-09-24

Regulatory Status

Discontinued

1986

24 Sep

Discontinued Application: 70483

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

Dosage Form

Strength

120MG

Approval Date

1986-09-24

70483 / 1 View Details

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70483

Product Number

Dosage Form

Strength

120MG

Approval Date

1986-09-24

Regulatory Status

Discontinued

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Drug Status Breakdown

58 total

Discontinued

Official Source

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

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Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

85794

Product Number

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

Strength

300MG;30MG

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