Solvay
FDA Approved Drugs

Solvay

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 73
  • Latest Approval Date Dec 05, 1994
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Solvay

Country

Germany

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Company Snapshot

Solvay

Rue de Ransbeek 310, Brussels, 1120

Germany

www.solvay.com/en/our-company View on Map
FDA Approved Drug Records ( 73 records )
1982
01 Jan
Discontinued Application: 16001

Drug Name

AQUATAG

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

16001 / 1

Active Ingredient

BENZTHIAZIDE

Application Number

16001

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16001

Drug Name

AQUATAG

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

16001 / 2

Active Ingredient

BENZTHIAZIDE

Application Number

16001

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
18 Apr
Discontinued Application: 84777

Drug Name

ARESTOCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

3%

Approval Date

1982-04-18

84777 / 2

Active Ingredient

MEPIVACAINE HYDROCHLORIDE

Application Number

84777

Product Number

2

Dosage Form

-

Strength

3%

Approval Date

1982-04-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85010

Drug Name

ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN

Product Number

1

Dosage Form

-

Strength

0.05MG/ML;2%

Approval Date

1982-01-01

85010 / 1

Active Ingredient

LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

Application Number

85010

Product Number

1

Dosage Form

-

Strength

0.05MG/ML;2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
03 Dec
Discontinued Application: 88041

Drug Name

BALNEOL-HC

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-12-03

88041 / 1

Active Ingredient

HYDROCORTISONE

Application Number

88041

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-12-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83606

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

16.2MG

Approval Date

1982-01-01

83606 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

83606

Product Number

1

Dosage Form

-

Strength

16.2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83896

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

97.2MG

Approval Date

1982-01-01

83896 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

83896

Product Number

1

Dosage Form

-

Strength

97.2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83897

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

48.6MG

Approval Date

1982-01-01

83897 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

83897

Product Number

1

Dosage Form

-

Strength

48.6MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83898

Drug Name

BUTABARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

32.4MG

Approval Date

1982-01-01

83898 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

83898

Product Number

1

Dosage Form

-

Strength

32.4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84932

Drug Name

CIN-QUIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84932 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

84932

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85296

Drug Name

CIN-QUIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

85296 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

85296

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85297

Drug Name

CIN-QUIN

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

85297 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

85297

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85298

Drug Name

CIN-QUIN

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

85298 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

85298

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85299

Drug Name

CIN-QUIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85299 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

85299

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85686

Drug Name

CURRETAB

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

85686 / 1

Active Ingredient

MEDROXYPROGESTERONE ACETATE

Application Number

85686

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84573

Drug Name

DERMACORT

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

84573 / 2

Active Ingredient

HYDROCORTISONE

Application Number

84573

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86462

Drug Name

DERMACORT

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86462 / 1

Active Ingredient

HYDROCORTISONE

Application Number

86462

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84991

Drug Name

DEXONE 0.5

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

84991 / 1

Active Ingredient

DEXAMETHASONE

Application Number

84991

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84993

Drug Name

DEXONE 0.75

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1982-01-01

84993 / 1

Active Ingredient

DEXAMETHASONE

Application Number

84993

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84990

Drug Name

DEXONE 1.5

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

1982-01-01

84990 / 1

Active Ingredient

DEXAMETHASONE

Application Number

84990

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84992

Drug Name

DEXONE 4

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

84992 / 1

Active Ingredient

DEXAMETHASONE

Application Number

84992

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
22 Mar
Discontinued Application: 72372

Drug Name

DUPHALAC

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1989-03-22

72372 / 1

Active Ingredient

LACTULOSE

Application Number

72372

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1989-03-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84436

Drug Name

ESTRAGUARD

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

84436 / 1

Active Ingredient

DIENESTROL

Application Number

84436

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83209

Drug Name

ESTRATAB

Product Number

1

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

83209 / 1

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83209

Product Number

1

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83856

Drug Name

ESTRATAB

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

83856 / 1

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83856

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83857

Drug Name

ESTRATAB

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

83857 / 1

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

83857

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86715

Drug Name

ESTRATAB

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

86715 / 1

Active Ingredient

ESTROGENS, ESTERIFIED

Application Number

86715

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17388

Drug Name

GYNOREST

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17388 / 1

Active Ingredient

DYDROGESTERONE

Application Number

17388

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17388

Drug Name

GYNOREST

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17388 / 2

Active Ingredient

DYDROGESTERONE

Application Number

17388

Product Number

2

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
08 Feb
Discontinued Application: 87213

Drug Name

HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG;50MG

Approval Date

1982-02-08

87213 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

87213

Product Number

1

Dosage Form

-

Strength

50MG;50MG

Approval Date

1982-02-08

Regulatory Status

Discontinued

1982
08 Feb
Discontinued Application: 87608

Drug Name

HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1982-02-08

87608 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

87608

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1982-02-08

Regulatory Status

Discontinued

1982
08 Feb
Discontinued Application: 87609

Drug Name

HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

100MG;50MG

Approval Date

1982-02-08

87609 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

87609

Product Number

1

Dosage Form

-

Strength

100MG;50MG

Approval Date

1982-02-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85323

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85323 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

85323

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17906

Drug Name

LACTULOSE

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1982-01-01

17906 / 1

Active Ingredient

LACTULOSE

Application Number

17906

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16782

Drug Name

LITHONATE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

16782 / 1

Active Ingredient

LITHIUM CARBONATE

Application Number

16782

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17672

Drug Name

LITHONATE

Product Number

1

Dosage Form

-

Strength

EQ 300MG CARBONATE/5ML

Approval Date

1982-01-01

17672 / 1

Active Ingredient

LITHIUM CITRATE

Application Number

17672

Product Number

1

Dosage Form

-

Strength

EQ 300MG CARBONATE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16980

Drug Name

LITHOTABS

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

16980 / 1

Active Ingredient

LITHIUM CARBONATE

Application Number

16980

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994
05 Dec
Discontinued Application: 20243

Drug Name

LUVOX

Product Number

1

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

20243 / 1

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

20243

Product Number

1

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

Regulatory Status

Discontinued

1994
05 Dec
Discontinued Application: 20243

Drug Name

LUVOX

Product Number

2

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

20243 / 2

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

20243

Product Number

2

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

Regulatory Status

Discontinued

1994
05 Dec
Discontinued Application: 20243

Drug Name

LUVOX

Product Number

3

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

20243 / 3

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

20243

Product Number

3

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

Regulatory Status

Discontinued

1994
05 Dec
Discontinued Application: 20243

Drug Name

LUVOX

Product Number

4

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

20243 / 4

Active Ingredient

FLUVOXAMINE MALEATE

Application Number

20243

Product Number

4

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84435

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84435 / 1

Active Ingredient

MEPROBAMATE

Application Number

84435

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84448

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84448 / 1

Active Ingredient

METHOCARBAMOL

Application Number

84448

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84449

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

84449 / 1

Active Ingredient

METHOCARBAMOL

Application Number

84449

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83009

Drug Name

ORASONE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

83009 / 1

Active Ingredient

PREDNISONE

Application Number

83009

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83009

Drug Name

ORASONE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

83009 / 2

Active Ingredient

PREDNISONE

Application Number

83009

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83009

Drug Name

ORASONE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

83009 / 3

Active Ingredient

PREDNISONE

Application Number

83009

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83009

Drug Name

ORASONE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

83009 / 4

Active Ingredient

PREDNISONE

Application Number

83009

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85999

Drug Name

ORASONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85999 / 1

Active Ingredient

PREDNISONE

Application Number

85999

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83993

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83993 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83993

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
22 Mar
Discontinued Application: 72374

Drug Name

PORTALAC

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1989-03-22

72374 / 1

Active Ingredient

LACTULOSE

Application Number

72374

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1989-03-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85685

Drug Name

PROVAL #3

Product Number

1

Dosage Form

-

Strength

325MG;30MG

Approval Date

1982-01-01

85685 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

85685

Product Number

1

Dosage Form

-

Strength

325MG;30MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
27 Nov
Discontinued Application: 89572

Drug Name

PYRIDOSTIGMINE BROMIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1990-11-27

89572 / 1

Active Ingredient

PYRIDOSTIGMINE BROMIDE

Application Number

89572

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1990-11-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61659

Drug Name

R-P MYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61659 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

61659

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80500

Drug Name

RAUWOLFIA SERPENTINA

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

80500 / 1

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80500

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80500

Drug Name

RAUWOLFIA SERPENTINA

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

80500 / 2

Active Ingredient

RAUWOLFIA SERPENTINA ROOT

Application Number

80500

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80446

Drug Name

RESERPINE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

80446 / 1

Active Ingredient

RESERPINE

Application Number

80446

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
28 Oct
Discontinued Application: 88376

Drug Name

RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1983-10-28

88376 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

88376

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1983-10-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61443

Drug Name

RETET

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61443 / 1

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61443

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 61443

Drug Name

RETET

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

61443 / 2

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61443

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83450

Drug Name

S.A.S.-500

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

83450 / 1

Active Ingredient

SULFASALAZINE

Application Number

83450

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87210

Drug Name

SER-A-GEN

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

87210 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

87210

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85897

Drug Name

SPRX-3

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

85897 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

85897

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80040

Drug Name

SULSOXIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80040 / 1

Active Ingredient

SULFISOXAZOLE

Application Number

80040

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
04 Sep
Discontinued Application: 71000

Drug Name

SYMADINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-09-04

71000 / 1

Active Ingredient

AMANTADINE HYDROCHLORIDE

Application Number

71000

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1986-09-04

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84035

Drug Name

TORA

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

84035 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

84035

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16249

Drug Name

TRANMEP

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

16249 / 1

Active Ingredient

MEPROBAMATE

Application Number

16249

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84369

Drug Name

TRANMEP

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

84369 / 1

Active Ingredient

MEPROBAMATE

Application Number

84369

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87113

Drug Name

TRIACORT

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

87113 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87113

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85893

Drug Name

UNIPRES

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

85893 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

85893

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86298

Drug Name

UNIPRES

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

86298 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

86298

Product Number

1

Dosage Form

-

Strength

25MG;15MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80992

Drug Name

VERMIDOL

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

80992 / 1

Active Ingredient

PIPERAZINE CITRATE

Application Number

80992

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83925

Drug Name

ZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83925 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83925

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
73 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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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

AQUATAG

Application Number

16001

Product Number

1

Active Ingredient

BENZTHIAZIDE

Dosage Form

-

Strength

25MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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