USL PHARMA
FDA Approved Drugs

USL PHARMA

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 105
  • Latest Approval Date Apr 17, 2002
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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Company

USL PHARMA

Country

United Kingdom

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USL PHARMA

United Kingdom

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FDA Approved Drug Records ( 105 records )
1982
22 Jun
Discontinued Application: 87919

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-06-22

87919 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

87919

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-06-22

Regulatory Status

Discontinued

1982
22 Jun
Discontinued Application: 87920

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-06-22

87920 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

87920

Product Number

1

Dosage Form

-

Strength

300MG;60MG

Approval Date

1982-06-22

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70753

Drug Name

ACETOHEXAMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-11-03

70753 / 1

Active Ingredient

ACETOHEXAMIDE

Application Number

70753

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1986
03 Nov
Discontinued Application: 70754

Drug Name

ACETOHEXAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-11-03

70754 / 1

Active Ingredient

ACETOHEXAMIDE

Application Number

70754

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-11-03

Regulatory Status

Discontinued

1982
10 Feb
Discontinued Application: 87775

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-02-10

87775 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

87775

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-02-10

Regulatory Status

Discontinued

1988
06 May
Discontinued Application: 71260

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-05-06

71260 / 1

Active Ingredient

BACLOFEN

Application Number

71260

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-05-06

Regulatory Status

Discontinued

1988
06 May
Discontinued Application: 71261

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-05-06

71261 / 1

Active Ingredient

BACLOFEN

Application Number

71261

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-05-06

Regulatory Status

Discontinued

1988
14 Jun
Discontinued Application: 89211

Drug Name

BENZTROPINE MESYLATE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1988-06-14

89211 / 1

Active Ingredient

BENZTROPINE MESYLATE

Application Number

89211

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1988-06-14

Regulatory Status

Discontinued

1988
14 Jun
Discontinued Application: 89212

Drug Name

BENZTROPINE MESYLATE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1988-06-14

89212 / 1

Active Ingredient

BENZTROPINE MESYLATE

Application Number

89212

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1988-06-14

Regulatory Status

Discontinued

1988
14 Jun
Discontinued Application: 89213

Drug Name

BENZTROPINE MESYLATE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1988-06-14

89213 / 1

Active Ingredient

BENZTROPINE MESYLATE

Application Number

89213

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1988-06-14

Regulatory Status

Discontinued

1983
25 Jan
Discontinued Application: 87964

Drug Name

BROMPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

2MG/5ML

Approval Date

1983-01-25

87964 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

87964

Product Number

1

Dosage Form

-

Strength

2MG/5ML

Approval Date

1983-01-25

Regulatory Status

Discontinued

1986
15 May
Discontinued Application: 70300

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1986-05-15

70300 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

70300

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1986-05-15

Regulatory Status

Discontinued

1988
12 Jan
Discontinued Application: 70477

Drug Name

CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE;5MG

Approval Date

1988-01-12

70477 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

Application Number

70477

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE;5MG

Approval Date

1988-01-12

Regulatory Status

Discontinued

1988
12 Jan
Discontinued Application: 70478

Drug Name

CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE;10MG

Approval Date

1988-01-12

70478 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

Application Number

70478

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE;10MG

Approval Date

1988-01-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84623

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84623 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84623

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84644

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84644 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84644

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84645

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84645 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

84645

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
30 Aug
Discontinued Application: 88708

Drug Name

CHLORPROPAMIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1984-08-30

88708 / 1

Active Ingredient

CHLORPROPAMIDE

Application Number

88708

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1984-08-30

Regulatory Status

Discontinued

1984
30 Aug
Discontinued Application: 88709

Drug Name

CHLORPROPAMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1984-08-30

88709 / 1

Active Ingredient

CHLORPROPAMIDE

Application Number

88709

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1984-08-30

Regulatory Status

Discontinued

1987
01 Jun
Discontinued Application: 89051

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1987-06-01

89051 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

89051

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1987-06-01

Regulatory Status

Discontinued

1987
01 Jun
Discontinued Application: 89052

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-06-01

89052 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

89052

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-06-01

Regulatory Status

Discontinued

1986
16 Jun
Discontinued Application: 70531

Drug Name

CLOFIBRATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-06-16

70531 / 1

Active Ingredient

CLOFIBRATE

Application Number

70531

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-06-16

Regulatory Status

Discontinued

1987
23 Jun
Discontinued Application: 71242

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1987-06-23

71242 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71242

Product Number

1

Dosage Form

-

Strength

3.75MG

Approval Date

1987-06-23

Regulatory Status

Discontinued

1987
23 Jun
Discontinued Application: 71243

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1987-06-23

71243 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71243

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

1987-06-23

Regulatory Status

Discontinued

1987
23 Jun
Discontinued Application: 71244

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-06-23

71244 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71244

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-06-23

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71864

Drug Name

DESIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1987-09-09

71864 / 1

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

71864

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71865

Drug Name

DESIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-09-09

71865 / 1

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

71865

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71866

Drug Name

DESIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1987-09-09

71866 / 1

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

71866

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1987
09 Sep
Discontinued Application: 71867

Drug Name

DESIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1987-09-09

71867 / 1

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

71867

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1987-09-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84640

Drug Name

DIPHEN

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

84640 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

84640

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
29 Mar
Discontinued Application: 87842

Drug Name

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-03-29

87842 / 1

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

87842

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-03-29

Regulatory Status

Discontinued

2002
17 Apr
Discontinued Application: 40297

Drug Name

ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2002-04-17

40297 / 1

Active Ingredient

ESTRADIOL

Application Number

40297

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2002-04-17

Regulatory Status

Discontinued

2002
17 Apr
Discontinued Application: 40297

Drug Name

ESTRADIOL

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2002-04-17

40297 / 2

Active Ingredient

ESTRADIOL

Application Number

40297

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2002-04-17

Regulatory Status

Discontinued

2002
17 Apr
Discontinued Application: 40297

Drug Name

ESTRADIOL

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2002-04-17

40297 / 3

Active Ingredient

ESTRADIOL

Application Number

40297

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2002-04-17

Regulatory Status

Discontinued

1988
17 Aug
Discontinued Application: 72362

Drug Name

FENOPROFEN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

1988-08-17

72362 / 1

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72362

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

1988-08-17

Regulatory Status

Discontinued

1985
08 Feb
Discontinued Application: 88742

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1985-02-08

88742 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88742

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1985-02-08

Regulatory Status

Discontinued

1985
28 Mar
Discontinued Application: 88756

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1985-03-28

88756 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88756

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1985-03-28

Regulatory Status

Discontinued

1985
11 Feb
Discontinued Application: 88757

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1985-02-11

88757 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88757

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1985-02-11

Regulatory Status

Discontinued

1987
09 Jul
Discontinued Application: 70562

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-07-09

70562 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

70562

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1987-07-09

Regulatory Status

Discontinued

1987
09 Jul
Discontinued Application: 70563

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-07-09

70563 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

70563

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1987-07-09

Regulatory Status

Discontinued

1982
13 May
Discontinued Application: 87828

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-05-13

87828 / 1

Active Ingredient

FOLIC ACID

Application Number

87828

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-05-13

Regulatory Status

Discontinued

1982
29 Mar
Discontinued Application: 87751

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-03-29

87751 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

87751

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-03-29

Regulatory Status

Discontinued

1982
29 Mar
Discontinued Application: 87780

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-03-29

87780 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

87780

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-03-29

Regulatory Status

Discontinued

1982
19 Apr
Discontinued Application: 87752

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-04-19

87752 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

87752

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-04-19

Regulatory Status

Discontinued

1982
19 Apr
Discontinued Application: 87827

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-04-19

87827 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

87827

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-04-19

Regulatory Status

Discontinued

1987
29 May
Discontinued Application: 89290

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-05-29

89290 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89290

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-05-29

Regulatory Status

Discontinued

1987
29 May
Discontinued Application: 89291

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-05-29

89291 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89291

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-05-29

Regulatory Status

Discontinued

1983
27 Sep
Discontinued Application: 88027

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-27

88027 / 1

Active Ingredient

HYDROCORTISONE

Application Number

88027

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-27

Regulatory Status

Discontinued

1983
27 Sep
Discontinued Application: 88029

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1983-09-27

88029 / 1

Active Ingredient

HYDROCORTISONE

Application Number

88029

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1983-09-27

Regulatory Status

Discontinued

1983
27 Sep
Discontinued Application: 88039

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1983-09-27

88039 / 1

Active Ingredient

HYDROCORTISONE

Application Number

88039

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

1983-09-27

Regulatory Status

Discontinued

1983
27 Sep
Discontinued Application: 88061

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-27

88061 / 1

Active Ingredient

HYDROCORTISONE

Application Number

88061

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-27

Regulatory Status

Discontinued

1983
26 Oct
Discontinued Application: 88195

Drug Name

HYDROFLUMETHIAZIDE AND RESERPINE

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1983-10-26

88195 / 1

Active Ingredient

HYDROFLUMETHIAZIDE; RESERPINE

Application Number

88195

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1983-10-26

Regulatory Status

Discontinued

1986
20 Mar
Discontinued Application: 89121

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-03-20

89121 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

89121

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-03-20

Regulatory Status

Discontinued

1986
20 Mar
Discontinued Application: 89122

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1986-03-20

89122 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

89122

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1986-03-20

Regulatory Status

Discontinued

1986
20 Mar
Discontinued Application: 89123

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1986-03-20

89123 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

89123

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1986-03-20

Regulatory Status

Discontinued

1982
10 Feb
Discontinued Application: 87776

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-02-10

87776 / 1

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

87776

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-02-10

Regulatory Status

Discontinued

1989
01 Feb
Discontinued Application: 72542

Drug Name

LITHIUM CARBONATE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1989-02-01

72542 / 1

Active Ingredient

LITHIUM CARBONATE

Application Number

72542

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1989-02-01

Regulatory Status

Discontinued

1986
22 Dec
Discontinued Application: 70539

Drug Name

LORAZEPAM

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-12-22

70539 / 1

Active Ingredient

LORAZEPAM

Application Number

70539

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1986-12-22

Regulatory Status

Discontinued

1986
22 Dec
Discontinued Application: 70540

Drug Name

LORAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-22

70540 / 1

Active Ingredient

LORAZEPAM

Application Number

70540

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-22

Regulatory Status

Discontinued

1988
25 Mar
Discontinued Application: 71007

Drug Name

MECLOFENAMATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1988-03-25

71007 / 1

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

71007

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1988-03-25

Regulatory Status

Discontinued

1988
25 Mar
Discontinued Application: 71008

Drug Name

MECLOFENAMATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1988-03-25

71008 / 1

Active Ingredient

MECLOFENAMATE SODIUM

Application Number

71008

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1988-03-25

Regulatory Status

Discontinued

1987
02 Oct
Discontinued Application: 70646

Drug Name

MEGESTROL ACETATE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-10-02

70646 / 1

Active Ingredient

MEGESTROL ACETATE

Application Number

70646

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-10-02

Regulatory Status

Discontinued

1987
02 Oct
Discontinued Application: 70647

Drug Name

MEGESTROL ACETATE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1987-10-02

70647 / 1

Active Ingredient

MEGESTROL ACETATE

Application Number

70647

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1987-10-02

Regulatory Status

Discontinued

1982
18 Mar
Discontinued Application: 87825

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-03-18

87825 / 1

Active Ingredient

MEPROBAMATE

Application Number

87825

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-03-18

Regulatory Status

Discontinued

1982
18 Mar
Discontinued Application: 87826

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-03-18

87826 / 1

Active Ingredient

MEPROBAMATE

Application Number

87826

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-03-18

Regulatory Status

Discontinued

1988
25 Jan
Discontinued Application: 71013

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-01-25

71013 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

71013

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-01-25

Regulatory Status

Discontinued

1988
25 Jan
Discontinued Application: 71014

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-01-25

71014 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

71014

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-01-25

Regulatory Status

Discontinued

1985
21 Mar
Discontinued Application: 88745

Drug Name

METHYCLOTHIAZIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-03-21

88745 / 1

Active Ingredient

METHYCLOTHIAZIDE

Application Number

88745

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-03-21

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80271

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

80271 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

80271

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
29 Jul
Discontinued Application: 70339

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-07-29

70339 / 1

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

70339

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-07-29

Regulatory Status

Discontinued

1988
16 Dec
Discontinued Application: 71537

Drug Name

MINOXIDIL

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1988-12-16

71537 / 1

Active Ingredient

MINOXIDIL

Application Number

71537

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1988-12-16

Regulatory Status

Discontinued

1983
04 Mar
Discontinued Application: 88116

Drug Name

MYFED

Product Number

1

Dosage Form

-

Strength

30MG/5ML;1.25MG/5ML

Approval Date

1983-03-04

88116 / 1

Active Ingredient

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

Application Number

88116

Product Number

1

Dosage Form

-

Strength

30MG/5ML;1.25MG/5ML

Approval Date

1983-03-04

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87963

Drug Name

MYIDYL

Product Number

1

Dosage Form

-

Strength

1.25MG/5ML

Approval Date

1983-01-18

87963 / 1

Active Ingredient

TRIPROLIDINE HYDROCHLORIDE

Application Number

87963

Product Number

1

Dosage Form

-

Strength

1.25MG/5ML

Approval Date

1983-01-18

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87996

Drug Name

MYMETHAZINE FORTIS

Product Number

1

Dosage Form

-

Strength

25MG/5ML

Approval Date

1983-01-18

87996 / 1

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

87996

Product Number

1

Dosage Form

-

Strength

25MG/5ML

Approval Date

1983-01-18

Regulatory Status

Discontinued

1988
10 Mar
Discontinued Application: 70746

Drug Name

OXYBUTYNIN CHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1988-03-10

70746 / 1

Active Ingredient

OXYBUTYNIN CHLORIDE

Application Number

70746

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1988-03-10

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83805

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

83805 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

83805

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84398

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

84398 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

84398

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83804

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

83804 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

83804

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
10 Dec
Discontinued Application: 88797

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-12-10

88797 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88797

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1984-12-10

Regulatory Status

Discontinued

1985
17 Jul
Discontinued Application: 88910

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1985-07-17

88910 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88910

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1985-07-17

Regulatory Status

Discontinued

1985
17 Jul
Discontinued Application: 88917

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1985-07-17

88917 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

88917

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1985-07-17

Regulatory Status

Discontinued

1987
06 Nov
Discontinued Application: 70427

Drug Name

PRAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1987-11-06

70427 / 1

Active Ingredient

PRAZEPAM

Application Number

70427

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1987-11-06

Regulatory Status

Discontinued

1987
06 Nov
Discontinued Application: 70428

Drug Name

PRAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-11-06

70428 / 1

Active Ingredient

PRAZEPAM

Application Number

70428

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1987-11-06

Regulatory Status

Discontinued

1982
14 Apr
Discontinued Application: 87837

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-04-14

87837 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

87837

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-04-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87651

Drug Name

SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1982-01-01

87651 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; SPIRONOLACTONE

Application Number

87651

Product Number

1

Dosage Form

-

Strength

25MG;25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
08 Nov
Discontinued Application: 70203

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1985-11-08

70203 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70203

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

1985-11-08

Regulatory Status

Discontinued

1985
08 Nov
Discontinued Application: 70204

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1985-11-08

70204 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70204

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1985-11-08

Regulatory Status

Discontinued

1986
01 Aug
Discontinued Application: 70063

Drug Name

SULMEPRIM

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1986-08-01

70063 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70063

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1986-08-01

Regulatory Status

Discontinued

1986
01 Aug
Discontinued Application: 70064

Drug Name

SULMEPRIM PEDIATRIC

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1986-08-01

70064 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70064

Product Number

1

Dosage Form

-

Strength

200MG/5ML;40MG/5ML

Approval Date

1986-08-01

Regulatory Status

Discontinued

1986
07 Jul
Discontinued Application: 70489

Drug Name

TEMAZEPAM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1986-07-07

70489 / 1

Active Ingredient

TEMAZEPAM

Application Number

70489

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1986-07-07

Regulatory Status

Discontinued

1986
07 Jul
Discontinued Application: 70490

Drug Name

TEMAZEPAM

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1986-07-07

70490 / 1

Active Ingredient

TEMAZEPAM

Application Number

70490

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1986-07-07

Regulatory Status

Discontinued

1989
11 Apr
Discontinued Application: 72001

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1989-04-11

72001 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

72001

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989
11 Apr
Discontinued Application: 72002

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1989-04-11

72002 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

72002

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989
11 Apr
Discontinued Application: 72003

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1989-04-11

72003 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

72003

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1989-04-11

Regulatory Status

Discontinued

1986
02 Apr
Discontinued Application: 70168

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-04-02

70168 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70168

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-04-02

Regulatory Status

Discontinued

1986
02 Apr
Discontinued Application: 70169

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-04-02

70169 / 1

Active Ingredient

TOLAZAMIDE

Application Number

70169

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1986-04-02

Regulatory Status

Discontinued

1988
11 Jan
Discontinued Application: 71355

Drug Name

TOLAZAMIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1988-01-11

71355 / 1

Active Ingredient

TOLAZAMIDE

Application Number

71355

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1988-01-11

Regulatory Status

Discontinued

1987
29 Apr
Discontinued Application: 70491

Drug Name

TRAZODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-04-29

70491 / 1

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

70491

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1987-04-29

Regulatory Status

Discontinued

1987
29 Apr
Discontinued Application: 70492

Drug Name

TRAZODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1987-04-29

70492 / 1

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

70492

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1987-04-29

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 71283

Drug Name

TRIMIPRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-12-08

71283 / 1

Active Ingredient

TRIMIPRAMINE MALEATE

Application Number

71283

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1987-12-08

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 71284

Drug Name

TRIMIPRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1987-12-08

71284 / 1

Active Ingredient

TRIMIPRAMINE MALEATE

Application Number

71284

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1987-12-08

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 71285

Drug Name

TRIMIPRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1987-12-08

71285 / 1

Active Ingredient

TRIMIPRAMINE MALEATE

Application Number

71285

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1987-12-08

Regulatory Status

Discontinued

1985
27 Jun
Discontinued Application: 88719

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-06-27

88719 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

88719

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1985-06-27

Regulatory Status

Discontinued

1985
06 Aug
Discontinued Application: 88720

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1985-08-06

88720 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

88720

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1985-08-06

Regulatory Status

Discontinued

1985
02 Jul
Discontinued Application: 88721

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-07-02

88721 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

88721

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1985-07-02

Regulatory Status

Discontinued

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Drug Status Breakdown
105 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

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

87919

Product Number

1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

-

Strength

300MG;30MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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