GD Searle LLC
FDA Approved Drugs

GD Searle LLC

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 Unclassified
  • Total Records 46
  • Latest Approval Date Dec 18, 1987
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
46
View
Unclassified
4
View
Discontinued
42
View
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Company

GD Searle LLC

Country

U.S.A

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GD Searle LLC

5200 Old Orchard Road Skokie, IL 60077

U.S.A

www.pfizer.com/ View on Map
FDA Approved Drug Records ( 46 records )
1982
01 Jan
Discontinued Application: 2386

Drug Name

AMINOPHYLLIN

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

2386 / 2

Active Ingredient

AMINOPHYLLINE

Application Number

2386

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 2386

Drug Name

AMINOPHYLLIN

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

2386 / 3

Active Ingredient

AMINOPHYLLINE

Application Number

2386

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
24 May
Discontinued Application: 87243

Drug Name

AMINOPHYLLIN

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-05-24

87243 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87243

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-05-24

Regulatory Status

Discontinued

1982
24 May
Discontinued Application: 87621

Drug Name

AMINOPHYLLIN

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-05-24

87621 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87621

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-05-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86205

Drug Name

AMMONIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

86205 / 1

Active Ingredient

AMMONIUM CHLORIDE

Application Number

86205

Product Number

1

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
30 Mar
Discontinued Application: 19038

Drug Name

CALAN

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1984-03-30

19038 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

19038

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1984-03-30

Regulatory Status

Discontinued

-
Unclassified Application: 21156

Drug Name

CELEBREX

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

21156 / 1

Active Ingredient

CELECOXIB

Application Number

21156

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21156

Drug Name

CELEBREX

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

21156 / 2

Active Ingredient

CELECOXIB

Application Number

21156

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21156

Drug Name

CELEBREX

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

-

21156 / 3

Active Ingredient

CELECOXIB

Application Number

21156

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

-

Regulatory Status

Unclassified

1987
18 Dec
Discontinued Application: 71727

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1987-12-18

71727 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71727

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1987-12-18

Regulatory Status

Discontinued

1987
18 Dec
Discontinued Application: 71728

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1987-12-18

71728 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71728

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1987-12-18

Regulatory Status

Discontinued

1987
18 Dec
Discontinued Application: 71729

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-12-18

71729 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71729

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-12-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17408

Drug Name

CU-7

Product Number

1

Dosage Form

-

Strength

89MG

Approval Date

1982-01-01

17408 / 1

Active Ingredient

COPPER

Application Number

17408

Product Number

1

Dosage Form

-

Strength

89MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18168

Drug Name

DEMULEN 1/35-21

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18168 / 1

Active Ingredient

ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE

Application Number

18168

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG **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: 18160

Drug Name

DEMULEN 1/35-28

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18160 / 1

Active Ingredient

ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE

Application Number

18160

Product Number

1

Dosage Form

-

Strength

0.035MG;1MG **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: 16927

Drug Name

DEMULEN 1/50-21

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

1982-01-01

16927 / 1

Active Ingredient

ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE

Application Number

16927

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16936

Drug Name

DEMULEN 1/50-28

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16936 / 1

Active Ingredient

ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE

Application Number

16936

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG **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: 18535

Drug Name

DIULO

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

18535 / 1

Active Ingredient

METOLAZONE

Application Number

18535

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18535

Drug Name

DIULO

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

18535 / 2

Active Ingredient

METOLAZONE

Application Number

18535

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18535

Drug Name

DIULO

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

18535 / 3

Active Ingredient

METOLAZONE

Application Number

18535

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10976

Drug Name

ENOVID

Product Number

4

Dosage Form

-

Strength

0.075MG;5MG

Approval Date

1982-01-01

10976 / 4

Active Ingredient

MESTRANOL; NORETHYNODREL

Application Number

10976

Product Number

4

Dosage Form

-

Strength

0.075MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10976

Drug Name

ENOVID

Product Number

5

Dosage Form

-

Strength

0.15MG;9.85MG

Approval Date

1982-01-01

10976 / 5

Active Ingredient

MESTRANOL; NORETHYNODREL

Application Number

10976

Product Number

5

Dosage Form

-

Strength

0.15MG;9.85MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10976

Drug Name

ENOVID

Product Number

8

Dosage Form

-

Strength

0.075MG;5MG

Approval Date

1982-01-01

10976 / 8

Active Ingredient

MESTRANOL; NORETHYNODREL

Application Number

10976

Product Number

8

Dosage Form

-

Strength

0.075MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10976

Drug Name

ENOVID-E

Product Number

6

Dosage Form

-

Strength

0.1MG;2.5MG

Approval Date

1982-01-01

10976 / 6

Active Ingredient

MESTRANOL; NORETHYNODREL

Application Number

10976

Product Number

6

Dosage Form

-

Strength

0.1MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10976

Drug Name

ENOVID-E 21

Product Number

7

Dosage Form

-

Strength

0.1MG;2.5MG

Approval Date

1982-01-01

10976 / 7

Active Ingredient

MESTRANOL; NORETHYNODREL

Application Number

10976

Product Number

7

Dosage Form

-

Strength

0.1MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83135

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

83135 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

83135

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83135

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

83135 / 2

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

83135

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 12699

Drug Name

LOMOTIL

Product Number

1

Dosage Form

-

Strength

0.025MG/5ML;2.5MG/5ML

Approval Date

1982-01-01

12699 / 1

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

12699

Product Number

1

Dosage Form

-

Strength

0.025MG/5ML;2.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86418

Drug Name

METARAMINOL BITARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1982-01-01

86418 / 1

Active Ingredient

METARAMINOL BITARTRATE

Application Number

86418

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86418

Drug Name

METARAMINOL BITARTRATE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1982-01-01

86418 / 2

Active Ingredient

METARAMINOL BITARTRATE

Application Number

86418

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16724

Drug Name

NORINYL 1+80 21-DAY

Product Number

1

Dosage Form

-

Strength

0.08MG;1MG

Approval Date

1982-01-01

16724 / 1

Active Ingredient

MESTRANOL; NORETHINDRONE

Application Number

16724

Product Number

1

Dosage Form

-

Strength

0.08MG;1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16725

Drug Name

NORINYL 1+80 28-DAY

Product Number

1

Dosage Form

-

Strength

0.08MG;1MG

Approval Date

1982-01-01

16725 / 1

Active Ingredient

MESTRANOL; NORETHINDRONE

Application Number

16725

Product Number

1

Dosage Form

-

Strength

0.08MG;1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

-
Unclassified Application: 17948

Drug Name

NORMINEST FE

Product Number

1

Dosage Form

-

Strength

0.035MG;0.5MG;75MG

Approval Date

-

17948 / 1

Active Ingredient

ETHINYL ESTRADIOL;NORETHINDRONE; FERROUS FUMARATE

Application Number

17948

Product Number

1

Dosage Form

-

Strength

0.035MG;0.5MG;75MG

Approval Date

-

Regulatory Status

Unclassified

1982
01 Jan
Discontinued Application: 16029

Drug Name

OVULEN

Product Number

2

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

16029 / 2

Active Ingredient

ETHYNODIOL DIACETATE; MESTRANOL

Application Number

16029

Product Number

2

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16029

Drug Name

OVULEN-21

Product Number

3

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

16029 / 3

Active Ingredient

ETHYNODIOL DIACETATE; MESTRANOL

Application Number

16029

Product Number

3

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16705

Drug Name

OVULEN-28

Product Number

1

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

16705 / 1

Active Ingredient

ETHYNODIOL DIACETATE; MESTRANOL

Application Number

16705

Product Number

1

Dosage Form

-

Strength

1MG;0.1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86219

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

1MEQ/ML

Approval Date

1982-01-01

86219 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86219

Product Number

1

Dosage Form

-

Strength

1MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86219

Drug Name

POTASSIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

86219 / 2

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86219

Product Number

2

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86219

Drug Name

POTASSIUM CHLORIDE

Product Number

3

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

86219 / 3

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86219

Product Number

3

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86219

Drug Name

POTASSIUM CHLORIDE

Product Number

4

Dosage Form

-

Strength

4MEQ/ML

Approval Date

1982-01-01

86219 / 4

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86219

Product Number

4

Dosage Form

-

Strength

4MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86220

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

86220 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86220

Product Number

1

Dosage Form

-

Strength

3MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86220

Drug Name

POTASSIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

86220 / 2

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86220

Product Number

2

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 8843

Drug Name

PRO-BANTHINE

Product Number

1

Dosage Form

-

Strength

30MG/VIAL

Approval Date

1982-01-01

8843 / 1

Active Ingredient

PROPANTHELINE BROMIDE

Application Number

8843

Product Number

1

Dosage Form

-

Strength

30MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86202

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86202 / 1

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

86202

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86202

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

86202 / 2

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

86202

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18205

Drug Name

TATUM-T

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1982-01-01

18205 / 1

Active Ingredient

COPPER

Application Number

18205

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
46 total
  • Discontinued
  • Unclassified
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

AMINOPHYLLIN

Application Number

2386

Product Number

2

Active Ingredient

AMINOPHYLLINE

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

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