PVT FORM Discontinued
FDA Approved Drugs

PVT FORM 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 44
Latest Approval Date Jul 24, 1986
Data Source FDA
First Approval Date Jan 01, 1982

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FDA Approved Drug Records ( 44 records )

1985

31 Jan

Discontinued Application: 88860

Drug Name

ALLERFED

Product Number

Dosage Form

Strength

60MG;2.5MG

Approval Date

1985-01-31

88860 / 1 View Details

Active Ingredient

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

Application Number

88860

Product Number

Dosage Form

Strength

60MG;2.5MG

Approval Date

1985-01-31

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83206

Drug Name

BENZTHIAZIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

83206 / 1 View Details

Active Ingredient

BENZTHIAZIDE

Application Number

83206

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80786

Drug Name

CHLORPHENIRAMINE MALEATE

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

80786 / 1 View Details

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

80786

Product Number

Dosage Form

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80340

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80340 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80340

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80340

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

80340 / 2 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80340

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80340

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

200MG

Approval Date

1982-01-01

80340 / 3 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

80340

Product Number

Dosage Form

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83420

Drug Name

DEXAMETHASONE

Product Number

Dosage Form

Strength

0.75MG

Approval Date

1982-01-01

83420 / 1 View Details

Active Ingredient

DEXAMETHASONE

Application Number

83420

Product Number

Dosage Form

Strength

0.75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85698

Drug Name

DI-METREX

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

85698 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85698

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83027

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

83027 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83027

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83027

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

83027 / 2 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83027

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85287

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1982-01-01

85287 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

85287

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85766

Drug Name

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Product Number

Dosage Form

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

85766 / 1 View Details

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

85766

Product Number

Dosage Form

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

24 Jul

Discontinued Application: 62631

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1986-07-24

62631 / 1 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62631

Product Number

Dosage Form

Strength

EQ 50MG BASE

Approval Date

1986-07-24

Regulatory Status

Discontinued

1986

24 Jul

Discontinued Application: 62631

Drug Name

DOXYCYCLINE HYCLATE

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1986-07-24

62631 / 2 View Details

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

62631

Product Number

Dosage Form

Strength

EQ 100MG BASE

Approval Date

1986-07-24

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83414

Drug Name

ESTERIFIED ESTROGENS

Product Number

Dosage Form

Strength

0.625MG

Approval Date

1982-01-01

83414 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83414

Product Number

Dosage Form

Strength

0.625MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83765

Drug Name

ESTERIFIED ESTROGENS

Product Number

Dosage Form

Strength

1.25MG

Approval Date

1982-01-01

83765 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83765

Product Number

Dosage Form

Strength

1.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85907

Drug Name

ESTERIFIED ESTROGENS

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

85907 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

85907

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85007

Drug Name

FEMOGEN

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

85007 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

85007

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85008

Drug Name

FEMOGEN

Product Number

Dosage Form

Strength

1.25MG

Approval Date

1982-01-01

85008 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

85008

Product Number

Dosage Form

Strength

1.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85076

Drug Name

FEMOGEN

Product Number

Dosage Form

Strength

0.625MG

Approval Date

1982-01-01

85076 / 1 View Details

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

85076

Product Number

Dosage Form

Strength

0.625MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86597

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

86597 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

86597

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 14601

Drug Name

MEPROBAMATE

Product Number

Dosage Form

Strength

400MG

Approval Date

1982-01-01

14601 / 1 View Details

Active Ingredient

MEPROBAMATE

Application Number

14601

Product Number

Dosage Form

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80970

Drug Name

METHSCOPOLAMINE BROMIDE

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

80970 / 1 View Details

Active Ingredient

METHSCOPOLAMINE BROMIDE

Application Number

80970

Product Number

Dosage Form

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80214

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

80214 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

80214

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80214

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

80214 / 2 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

80214

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80214

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80214 / 3 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

80214

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83836

Drug Name

METHYLTESTOSTERONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

83836 / 1 View Details

Active Ingredient

METHYLTESTOSTERONE

Application Number

83836

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85199

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

85199 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85199

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85697

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

85697 / 1 View Details

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85697

Product Number

Dosage Form

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80211

Drug Name

PREDNISOLONE

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

80211 / 1 View Details

Active Ingredient

PREDNISOLONE

Application Number

80211

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85151

Drug Name

PREDNISONE

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

85151 / 1 View Details

Active Ingredient

PREDNISONE

Application Number

85151

Product Number

Dosage Form

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83214

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

12.5MG

Approval Date

1982-01-01

83214 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83214

Product Number

Dosage Form

Strength

12.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83658

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

83658 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83658

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80977

Drug Name

PROPANTHELINE BROMIDE

Product Number

Dosage Form

Strength

15MG

Approval Date

1982-01-01

80977 / 1 View Details

Active Ingredient

PROPANTHELINE BROMIDE

Application Number

80977

Product Number

Dosage Form

Strength

15MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83113

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

83113 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83113

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83464

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

Dosage Form

Strength

32MG

Approval Date

1982-01-01

83464 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83464

Product Number

Dosage Form

Strength

32MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80583

Drug Name

RAUWOLFIA SERPENTINA

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

80583 / 1 View Details

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80583

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80583

Drug Name

RAUWOLFIA SERPENTINA

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

80583 / 2 View Details

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80583

Product Number

Dosage Form

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80582

Drug Name

RESERPINE

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

80582 / 1 View Details

Active Ingredient

RESERPINE

Application Number

80582

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80582

Drug Name

RESERPINE

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

80582 / 2 View Details

Active Ingredient

RESERPINE

Application Number

80582

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85775

Drug Name

RESERPINE

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

85775 / 1 View Details

Active Ingredient

RESERPINE

Application Number

85775

Product Number

Dosage Form

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86117

Drug Name

RESERPINE

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1982-01-01

86117 / 1 View Details

Active Ingredient

RESERPINE

Application Number

86117

Product Number

Dosage Form

Strength

0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

24 Jul

Discontinued Application: 62686

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-07-24

62686 / 1 View Details

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62686

Product Number

Dosage Form

Strength

250MG

Approval Date

1986-07-24

Regulatory Status

Discontinued

1986

24 Jul

Discontinued Application: 62686

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1986-07-24

62686 / 2 View Details

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

62686

Product Number

Dosage Form

Strength

500MG

Approval Date

1986-07-24

Regulatory Status

Discontinued

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Drug Status Breakdown

44 total

Discontinued

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Drug Name

ALLERFED

Application Number

88860

Product Number

Active Ingredient

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

Dosage Form

Strength

60MG;2.5MG

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