ABRAXIS PHARM
FDA Approved Drugs

ABRAXIS PHARM

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 RX
  • Total Records 142
  • Latest Approval Date Dec 22, 1989
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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Discontinued
141
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Company

ABRAXIS PHARM

Country

U.S.A

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ABRAXIS PHARM

U.S.A

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FDA Approved Drug Records ( 142 records )
1986
17 Jun
Discontinued Application: 70522

Drug Name

AMINOCAPROIC ACID

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1986-06-17

70522 / 1

Active Ingredient

AMINOCAPROIC ACID

Application Number

70522

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1986-06-17

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84568

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

84568 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

84568

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87200

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

87200 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87200

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
06 Jan
Discontinued Application: 87250

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-06

87250 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87250

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-06

Regulatory Status

Discontinued

1983
30 Aug
Discontinued Application: 87886

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1983-08-30

87886 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87886

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1983-08-30

Regulatory Status

Discontinued

1984
25 Jan
Discontinued Application: 88407

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1984-01-25

88407 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

88407

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1984-01-25

Regulatory Status

Discontinued

1987
13 Apr
Discontinued Application: 62728

Drug Name

AMPHOTERICIN B

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1987-04-13

62728 / 1

Active Ingredient

AMPHOTERICIN B

Application Number

62728

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1987-04-13

Regulatory Status

Discontinued

1985
07 Feb
Discontinued Application: 88909

Drug Name

BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

270MG/30ML (9MG/ML)

Approval Date

1985-02-07

88909 / 1

Active Ingredient

SODIUM CHLORIDE

Application Number

88909

Product Number

1

Dosage Form

-

Strength

270MG/30ML (9MG/ML)

Approval Date

1985-02-07

Regulatory Status

Discontinued

1985
15 May
Discontinued Application: 88909

Drug Name

BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

1985-05-15

88909 / 2

Active Ingredient

SODIUM CHLORIDE

Application Number

88909

Product Number

2

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

1985-05-15

Regulatory Status

Discontinued

1987
29 Dec
Discontinued Application: 89099

Drug Name

BACTERIOSTATIC WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1987-12-29

89099 / 1

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

89099

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1987-12-29

Regulatory Status

Discontinued

1987
29 Dec
Discontinued Application: 89100

Drug Name

BACTERIOSTATIC WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1987-12-29

89100 / 1

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

89100

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1987-12-29

Regulatory Status

Discontinued

1986
29 Apr
Discontinued Application: 70134

Drug Name

BRETYLIUM TOSYLATE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-04-29

70134 / 1

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

70134

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1987
13 Feb
Discontinued Application: 71298

Drug Name

BRETYLIUM TOSYLATE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1987-02-13

71298 / 1

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

71298

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1987-02-13

Regulatory Status

Discontinued

1987
30 Apr
Discontinued Application: 89373

Drug Name

CALCIUM GLUCEPTATE

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1987-04-30

89373 / 1

Active Ingredient

CALCIUM GLUCEPTATE

Application Number

89373

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1987-04-30

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62688

Drug Name

CEFAZOLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-17

62688 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

62688

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62688

Drug Name

CEFAZOLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-17

62688 / 3

Active Ingredient

CEFAZOLIN SODIUM

Application Number

62688

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62688

Drug Name

CEFAZOLIN SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

1986-11-17

62688 / 4

Active Ingredient

CEFAZOLIN SODIUM

Application Number

62688

Product Number

4

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1987
03 Aug
Discontinued Application: 62688

Drug Name

CEFAZOLIN SODIUM

Product Number

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-08-03

62688 / 5

Active Ingredient

CEFAZOLIN SODIUM

Application Number

62688

Product Number

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-08-03

Regulatory Status

Discontinued

1987
10 Jun
Discontinued Application: 62666

Drug Name

CEPHALOTHIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1987-06-10

62666 / 1

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62666

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1987-06-10

Regulatory Status

Discontinued

1987
10 Jun
Discontinued Application: 62666

Drug Name

CEPHALOTHIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-06-10

62666 / 2

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62666

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-06-10

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62723

Drug Name

CEPHAPIRIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-17

62723 / 1

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62723

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62723

Drug Name

CEPHAPIRIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-17

62723 / 2

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62723

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62723

Drug Name

CEPHAPIRIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1986-11-17

62723 / 3

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62723

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62723

Drug Name

CEPHAPIRIN SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1986-11-17

62723 / 4

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62723

Product Number

4

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 62723

Drug Name

CEPHAPIRIN SODIUM

Product Number

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1986-11-17

62723 / 5

Active Ingredient

CEPHAPIRIN SODIUM

Application Number

62723

Product Number

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1986-11-17

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84911

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

84911 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84911

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
05 May
Discontinued Application: 19271

Drug Name

CHROMIC CHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.004MG CHROMIUM/ML

Approval Date

1987-05-05

19271 / 1

Active Ingredient

CHROMIC CHLORIDE

Application Number

19271

Product Number

1

Dosage Form

-

Strength

EQ 0.004MG CHROMIUM/ML

Approval Date

1987-05-05

Regulatory Status

Discontinued

1988
03 Jun
Discontinued Application: 62747

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1988-06-03

62747 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62747

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1988-06-03

Regulatory Status

Discontinued

1989
22 Dec
RX Application: 50635

Drug Name

CLINDAMYCIN PHOSPHATE IN DEXTROSE 5%

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/100ML

Approval Date

1989-12-22

50635 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

50635

Product Number

1

Dosage Form

-

Strength

EQ 900MG BASE/100ML

Approval Date

1989-12-22

Regulatory Status

RX

1989
22 Dec
Discontinued Application: 50636

Drug Name

CLINDAMYCIN PHOSPHATE IN DEXTROSE 5%

Product Number

1

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

1989-12-22

50636 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

50636

Product Number

1

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

1989-12-22

Regulatory Status

Discontinued

1987
05 May
Discontinued Application: 19350

Drug Name

CUPRIC SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-05-05

19350 / 1

Active Ingredient

CUPRIC SULFATE

Application Number

19350

Product Number

1

Dosage Form

-

Strength

EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-05-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80510

Drug Name

CYANOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

0.1MG/ML

Approval Date

1982-01-01

80510 / 1

Active Ingredient

CYANOCOBALAMIN

Application Number

80510

Product Number

1

Dosage Form

-

Strength

0.1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80510

Drug Name

CYANOCOBALAMIN

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

80510 / 2

Active Ingredient

CYANOCOBALAMIN

Application Number

80510

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80510

Drug Name

CYANOCOBALAMIN

Product Number

3

Dosage Form

-

Strength

0.03MG/ML

Approval Date

1982-01-01

80510 / 3

Active Ingredient

CYANOCOBALAMIN

Application Number

80510

Product Number

3

Dosage Form

-

Strength

0.03MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
28 Aug
Discontinued Application: 70962

Drug Name

DACARBAZINE

Product Number

1

Dosage Form

-

Strength

100MG/VIAL

Approval Date

1986-08-28

70962 / 1

Active Ingredient

DACARBAZINE

Application Number

70962

Product Number

1

Dosage Form

-

Strength

100MG/VIAL

Approval Date

1986-08-28

Regulatory Status

Discontinued

1986
28 Aug
Discontinued Application: 70990

Drug Name

DACARBAZINE

Product Number

1

Dosage Form

-

Strength

200MG/VIAL

Approval Date

1986-08-28

70990 / 1

Active Ingredient

DACARBAZINE

Application Number

70990

Product Number

1

Dosage Form

-

Strength

200MG/VIAL

Approval Date

1986-08-28

Regulatory Status

Discontinued

1984
25 Jan
Discontinued Application: 88448

Drug Name

DEXAMETHASONE

Product Number

1

Dosage Form

-

Strength

EQ 4MG PHOSPHATE/ML

Approval Date

1984-01-25

88448 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE

Application Number

88448

Product Number

1

Dosage Form

-

Strength

EQ 4MG PHOSPHATE/ML

Approval Date

1984-01-25

Regulatory Status

Discontinued

1986
25 Jun
Discontinued Application: 70662

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1986-06-25

70662 / 1

Active Ingredient

DIAZEPAM

Application Number

70662

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1986-06-25

Regulatory Status

Discontinued

1987
26 Aug
Discontinued Application: 71519

Drug Name

DIAZOXIDE

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

1987-08-26

71519 / 1

Active Ingredient

DIAZOXIDE

Application Number

71519

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

1987-08-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83217

Drug Name

DIGOXIN

Product Number

1

Dosage Form

-

Strength

0.25MG/ML

Approval Date

1982-01-01

83217 / 1

Active Ingredient

DIGOXIN

Application Number

83217

Product Number

1

Dosage Form

-

Strength

0.25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80586

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE PRESERVATIVE FREE

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

80586 / 2

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80586

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
12 Jun
Discontinued Application: 70012

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-06-12

70012 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70012

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-06-12

Regulatory Status

Discontinued

1985
12 Jun
Discontinued Application: 70013

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-06-12

70013 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70013

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-06-12

Regulatory Status

Discontinued

1985
20 Mar
Discontinued Application: 70058

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-03-20

70058 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70058

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1985-03-20

Regulatory Status

Discontinued

1985
20 Mar
Discontinued Application: 70059

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-03-20

70059 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70059

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1985-03-20

Regulatory Status

Discontinued

1985
04 Dec
Discontinued Application: 70364

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

160MG/ML

Approval Date

1985-12-04

70364 / 1

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70364

Product Number

1

Dosage Form

-

Strength

160MG/ML

Approval Date

1985-12-04

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 70992

Drug Name

DROPERIDOL

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-11-17

70992 / 1

Active Ingredient

DROPERIDOL

Application Number

70992

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 70993

Drug Name

DROPERIDOL

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-11-17

70993 / 1

Active Ingredient

DROPERIDOL

Application Number

70993

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
24 Nov
Discontinued Application: 62604

Drug Name

ERYTHROMYCIN LACTOBIONATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-24

62604 / 1

Active Ingredient

ERYTHROMYCIN LACTOBIONATE

Application Number

62604

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-11-24

Regulatory Status

Discontinued

1986
24 Nov
Discontinued Application: 62604

Drug Name

ERYTHROMYCIN LACTOBIONATE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-24

62604 / 2

Active Ingredient

ERYTHROMYCIN LACTOBIONATE

Application Number

62604

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-11-24

Regulatory Status

Discontinued

1986
21 Mar
Discontinued Application: 89152

Drug Name

FLUOROURACIL

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-03-21

89152 / 1

Active Ingredient

FLUOROURACIL

Application Number

89152

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-03-21

Regulatory Status

Discontinued

1987
12 Jan
Discontinued Application: 89428

Drug Name

FLUOROURACIL

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1987-01-12

89428 / 1

Active Ingredient

FLUOROURACIL

Application Number

89428

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1987-01-12

Regulatory Status

Discontinued

1987
12 Mar
Discontinued Application: 89519

Drug Name

FLUOROURACIL

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1987-03-12

89519 / 1

Active Ingredient

FLUOROURACIL

Application Number

89519

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1987-03-12

Regulatory Status

Discontinued

1982
30 Jul
Discontinued Application: 18507

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-07-30

18507 / 1

Active Ingredient

FUROSEMIDE

Application Number

18507

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1982-07-30

Regulatory Status

Discontinued

1984
13 Aug
Discontinued Application: 19036

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1984-08-13

19036 / 1

Active Ingredient

FUROSEMIDE

Application Number

19036

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1984-08-13

Regulatory Status

Discontinued

1984
12 Jun
Discontinued Application: 88475

Drug Name

GLYCOPYRROLATE

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1984-06-12

88475 / 1

Active Ingredient

GLYCOPYRROLATE

Application Number

88475

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1984-06-12

Regulatory Status

Discontinued

1987
20 Jan
Discontinued Application: 71187

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-01-20

71187 / 1

Active Ingredient

HALOPERIDOL LACTATE

Application Number

71187

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1987-01-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17033

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

17033 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

17033

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17979

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

17979 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

17979

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17979

Drug Name

HEPARIN SODIUM

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

17979 / 2

Active Ingredient

HEPARIN SODIUM

Application Number

17979

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17979

Drug Name

HEPARIN SODIUM

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

17979 / 3

Active Ingredient

HEPARIN SODIUM

Application Number

17979

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
11 Aug
Discontinued Application: 89532

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1987-08-11

89532 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

89532

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

1987-08-11

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88667

Drug Name

HYDROCORTISONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1984-06-08

88667 / 1

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

88667

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88668

Drug Name

HYDROCORTISONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1984-06-08

88668 / 1

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

88668

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88669

Drug Name

HYDROCORTISONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-06-08

88669 / 1

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

88669

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88670

Drug Name

HYDROCORTISONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1984-06-08

88670 / 1

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

88670

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88712

Drug Name

HYDROCORTISONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1984-06-08

88712 / 1

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

88712

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84921

Drug Name

HYDROXOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

84921 / 1

Active Ingredient

HYDROXOCOBALAMIN

Application Number

84921

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83431

Drug Name

ISOPROTERENOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1982-01-01

83431 / 1

Active Ingredient

ISOPROTERENOL HYDROCHLORIDE

Application Number

83431

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
05 Apr
Discontinued Application: 62504

Drug Name

KANAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1984-04-05

62504 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62504

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1984-04-05

Regulatory Status

Discontinued

1984
05 Apr
Discontinued Application: 62504

Drug Name

KANAMYCIN SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1984-04-05

62504 / 2

Active Ingredient

KANAMYCIN SULFATE

Application Number

62504

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1984-04-05

Regulatory Status

Discontinued

1984
05 Apr
Discontinued Application: 62504

Drug Name

KANAMYCIN SULFATE

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1984-04-05

62504 / 3

Active Ingredient

KANAMYCIN SULFATE

Application Number

62504

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1984-04-05

Regulatory Status

Discontinued

1986
01 Dec
Discontinued Application: 88939

Drug Name

LEUCOVORIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1986-12-01

88939 / 1

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

88939

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1986-12-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17508

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

17508 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

17508

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17508

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

4%

Approval Date

1982-01-01

17508 / 2

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

17508

Product Number

2

Dosage Form

-

Strength

4%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17508

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

20%

Approval Date

1982-01-01

17508 / 4

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

17508

Product Number

4

Dosage Form

-

Strength

20%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80420

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80420 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

80420

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80420

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

80420 / 2

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

80420

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80420

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

80420 / 4

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

80420

Product Number

4

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80420

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

1.5%

Approval Date

1982-01-01

80420 / 5

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

80420

Product Number

5

Dosage Form

-

Strength

1.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86761

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86761 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

86761

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86761

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

86761 / 2

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

86761

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
08 Aug
Discontinued Application: 18440

Drug Name

M.V.C. 9+3

Product Number

2

Dosage Form

-

Strength

10MG/ML;0.006MG/ML;0.5MCG/ML;1.5MG/ML;20 IU/ML;0.04MG/ML;4MG/ML;0.4MG/ML;0.36MG/ML;0.3MG/ML;330 UNITS/ML;1 IU/ML

Approval Date

1985-08-08

18440 / 2

Active Ingredient

ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E

Application Number

18440

Product Number

2

Dosage Form

-

Strength

10MG/ML;0.006MG/ML;0.5MCG/ML;1.5MG/ML;20 IU/ML;0.04MG/ML;4MG/ML;0.4MG/ML;0.36MG/ML;0.3MG/ML;330 UNITS/ML;1 IU/ML

Approval Date

1985-08-08

Regulatory Status

Discontinued

1987
05 May
Discontinued Application: 19228

Drug Name

MANGANESE SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG MANGANESE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-05-05

19228 / 1

Active Ingredient

MANGANESE SULFATE

Application Number

19228

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG MANGANESE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-05-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86754

Drug Name

MANNITOL 25%

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML

Approval Date

1982-01-01

86754 / 1

Active Ingredient

MANNITOL

Application Number

86754

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80431

Drug Name

METARAMINOL BITARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1982-01-01

80431 / 1

Active Ingredient

METARAMINOL BITARTRATE

Application Number

80431

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
11 Oct
Discontinued Application: 88935

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/VIAL

Approval Date

1985-10-11

88935 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

88935

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/VIAL

Approval Date

1985-10-11

Regulatory Status

Discontinued

1985
11 Oct
Discontinued Application: 88936

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1985-10-11

88936 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

88936

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1985-10-11

Regulatory Status

Discontinued

1985
11 Oct
Discontinued Application: 88937

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1985-10-11

88937 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

88937

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1985-10-11

Regulatory Status

Discontinued

1986
13 Jun
Discontinued Application: 89263

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1986-06-13

89263 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89263

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1986-06-13

Regulatory Status

Discontinued

1986
13 Jun
Discontinued Application: 89322

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1986-06-13

89322 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89322

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1986-06-13

Regulatory Status

Discontinued

1986
13 Jun
Discontinued Application: 89323

Drug Name

METHOTREXATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE/ML

Approval Date

1986-06-13

89323 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89323

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE/ML

Approval Date

1986-06-13

Regulatory Status

Discontinued

1986
03 Jun
Discontinued Application: 70652

Drug Name

METHYLDOPATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-06-03

70652 / 1

Active Ingredient

METHYLDOPATE HYDROCHLORIDE

Application Number

70652

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-06-03

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88676

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1984-06-08

88676 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

88676

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88677

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1984-06-08

88677 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

88677

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88678

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-06-08

88678 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

88678

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1984
08 Jun
Discontinued Application: 88679

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1984-06-08

88679 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

88679

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1984-06-08

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89143

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1986-03-28

89143 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89143

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89144

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1986-03-28

89144 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89144

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89186

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-03-28

89186 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89186

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89187

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-03-28

89187 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89187

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89188

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-28

89188 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89188

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1986
28 Mar
Discontinued Application: 89189

Drug Name

METHYLPREDNISOLONE SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-28

89189 / 1

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89189

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-28

Regulatory Status

Discontinued

1984
03 Dec
Discontinued Application: 70071

Drug Name

METRONIDAZOLE

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1984-12-03

70071 / 1

Active Ingredient

METRONIDAZOLE

Application Number

70071

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1984-12-03

Regulatory Status

Discontinued

1985
15 Oct
Discontinued Application: 70295

Drug Name

METRONIDAZOLE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1985-10-15

70295 / 1

Active Ingredient

METRONIDAZOLE HYDROCHLORIDE

Application Number

70295

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1985-10-15

Regulatory Status

Discontinued

1986
02 Jul
Discontinued Application: 70751

Drug Name

NALBUPHINE

Product Number

1

Dosage Form

-

Strength

10MG/ML (10MG/ML)

Approval Date

1986-07-02

70751 / 1

Active Ingredient

NALBUPHINE HYDROCHLORIDE

Application Number

70751

Product Number

1

Dosage Form

-

Strength

10MG/ML (10MG/ML)

Approval Date

1986-07-02

Regulatory Status

Discontinued

1986
24 Sep
Discontinued Application: 70752

Drug Name

NALBUPHINE

Product Number

1

Dosage Form

-

Strength

20MG/ML (20MG/ML)

Approval Date

1986-09-24

70752 / 1

Active Ingredient

NALBUPHINE HYDROCHLORIDE

Application Number

70752

Product Number

1

Dosage Form

-

Strength

20MG/ML (20MG/ML)

Approval Date

1986-09-24

Regulatory Status

Discontinued

1986
24 Sep
Discontinued Application: 70752

Drug Name

NALBUPHINE

Product Number

2

Dosage Form

-

Strength

200MG/10ML (20MG/ML)

Approval Date

1986-09-24

70752 / 2

Active Ingredient

NALBUPHINE HYDROCHLORIDE

Application Number

70752

Product Number

2

Dosage Form

-

Strength

200MG/10ML (20MG/ML)

Approval Date

1986-09-24

Regulatory Status

Discontinued

1986
02 Jul
Discontinued Application: 70751

Drug Name

NALBUPHINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

1986-07-02

70751 / 2

Active Ingredient

NALBUPHINE HYDROCHLORIDE

Application Number

70751

Product Number

2

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

1986-07-02

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 70648

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.02MG/ML

Approval Date

1986-11-17

70648 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

70648

Product Number

1

Dosage Form

-

Strength

0.02MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 70649

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

1986-11-17

70649 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

70649

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 70661

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.02MG/ML

Approval Date

1986-11-17

70661 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

70661

Product Number

1

Dosage Form

-

Strength

0.02MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1988
16 Dec
Discontinued Application: 71604

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-12-16

71604 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

71604

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1988-12-16

Regulatory Status

Discontinued

1983
03 Oct
Discontinued Application: 88290

Drug Name

NANDROLONE DECANOATE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1983-10-03

88290 / 1

Active Ingredient

NANDROLONE DECANOATE

Application Number

88290

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1983-10-03

Regulatory Status

Discontinued

1983
14 Oct
Discontinued Application: 88317

Drug Name

NANDROLONE DECANOATE

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

1983-10-14

88317 / 1

Active Ingredient

NANDROLONE DECANOATE

Application Number

88317

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

1983-10-14

Regulatory Status

Discontinued

1985
13 Dec
Discontinued Application: 70077

Drug Name

NITROGLYCERIN

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1985-12-13

70077 / 1

Active Ingredient

NITROGLYCERIN

Application Number

70077

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1985-12-13

Regulatory Status

Discontinued

1987
08 May
Discontinued Application: 71203

Drug Name

NITROGLYCERIN

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-05-08

71203 / 1

Active Ingredient

NITROGLYCERIN

Application Number

71203

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1987-05-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80204

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

80204 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

80204

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84290

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

84290 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

84290

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86713

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

86713 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86713

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86714

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

86714 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

86714

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
20 Apr
Discontinued Application: 87787

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-04-20

87787 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

87787

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-04-20

Regulatory Status

Discontinued

1983
03 Feb
Discontinued Application: 87885

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1983-02-03

87885 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

87885

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1983-02-03

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 89415

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1986-11-17

89415 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

89415

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1986
17 Nov
Discontinued Application: 89416

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1986-11-17

89416 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

89416

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1986-11-17

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80384

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80384 / 2

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

80384

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80384

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

80384 / 3

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

80384

Product Number

3

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80421

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80421 / 1

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

80421

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80421

Drug Name

PROCAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

80421 / 2

Active Ingredient

PROCAINE HYDROCHLORIDE

Application Number

80421

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
23 Jul
Discontinued Application: 71188

Drug Name

RITODRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1987-07-23

71188 / 1

Active Ingredient

RITODRINE HYDROCHLORIDE

Application Number

71188

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1987-07-23

Regulatory Status

Discontinued

1987
23 Jul
Discontinued Application: 71189

Drug Name

RITODRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

1987-07-23

71189 / 1

Active Ingredient

RITODRINE HYDROCHLORIDE

Application Number

71189

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

1987-07-23

Regulatory Status

Discontinued

1987
22 Apr
Discontinued Application: 19329

Drug Name

SODIUM CHLORIDE 23.4% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

234MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-04-22

19329 / 1

Active Ingredient

SODIUM CHLORIDE

Application Number

19329

Product Number

1

Dosage Form

-

Strength

234MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-04-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17033

Drug Name

SODIUM HEPARIN

Product Number

2

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

17033 / 2

Active Ingredient

HEPARIN SODIUM

Application Number

17033

Product Number

2

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17033

Drug Name

SODIUM HEPARIN

Product Number

3

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

17033 / 3

Active Ingredient

HEPARIN SODIUM

Application Number

17033

Product Number

3

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17033

Drug Name

SODIUM HEPARIN

Product Number

4

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

1982-01-01

17033 / 4

Active Ingredient

HEPARIN SODIUM

Application Number

17033

Product Number

4

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
17 Jan
Discontinued Application: 70031

Drug Name

SODIUM NITROPRUSSIDE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1985-01-17

70031 / 1

Active Ingredient

SODIUM NITROPRUSSIDE

Application Number

70031

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1985-01-17

Regulatory Status

Discontinued

1987
29 Dec
Discontinued Application: 70223

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

80MG/ML;16MG/ML

Approval Date

1987-12-29

70223 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70223

Product Number

1

Dosage Form

-

Strength

80MG/ML;16MG/ML

Approval Date

1987-12-29

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80509

Drug Name

THIAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

80509 / 1

Active Ingredient

THIAMINE HYDROCHLORIDE

Application Number

80509

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
01 May
Discontinued Application: 70348

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-05-01

70348 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70348

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1986-05-01

Regulatory Status

Discontinued

1985
18 Nov
Discontinued Application: 89011

Drug Name

VINBLASTINE SULFATE

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1985-11-18

89011 / 1

Active Ingredient

VINBLASTINE SULFATE

Application Number

89011

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1985-11-18

Regulatory Status

Discontinued

1986
10 Sep
Discontinued Application: 70411

Drug Name

VINCRISTINE SULFATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1986-09-10

70411 / 1

Active Ingredient

VINCRISTINE SULFATE

Application Number

70411

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1986-09-10

Regulatory Status

Discontinued

1987
05 May
Discontinued Application: 19229

Drug Name

ZINC SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 1MG ZINC/ML

Approval Date

1987-05-05

19229 / 2

Active Ingredient

ZINC SULFATE

Application Number

19229

Product Number

2

Dosage Form

-

Strength

EQ 1MG ZINC/ML

Approval Date

1987-05-05

Regulatory Status

Discontinued

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Drug Status Breakdown
142 total
  • Discontinued
  • RX
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

AMINOCAPROIC ACID

Application Number

70522

Product Number

1

Active Ingredient

AMINOCAPROIC ACID

Dosage Form

-

Strength

250MG/ML

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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Searchable pharmaceutical data

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