Abbott Laboratories

1982

01 Jan

Discontinued Application: 85928

Drug Name

A-HYDROCORT

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1982-01-01

85928 / 1 View Details

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

85928

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 89577

Drug Name

A-HYDROCORT

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1989-04-11

89577 / 1 View Details

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

89577

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 89578

Drug Name

A-HYDROCORT

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1989-04-11

89578 / 1 View Details

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

89578

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 89579

Drug Name

A-HYDROCORT

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1989-04-11

89579 / 1 View Details

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

89579

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1989-04-11

Regulatory Status

Discontinued

1989

11 Apr

Discontinued Application: 89580

Drug Name

A-HYDROCORT

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1989-04-11

89580 / 1 View Details

Active Ingredient

HYDROCORTISONE SODIUM SUCCINATE

Application Number

89580

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1989-04-11

Regulatory Status

Discontinued

1991

22 Feb

Discontinued Application: 89573

Drug Name

A-METHAPRED

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1991-02-22

89573 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89573

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

1991-02-22

Regulatory Status

Discontinued

1991

22 Feb

Discontinued Application: 89574

Drug Name

A-METHAPRED

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1991-02-22

89574 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89574

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1991-02-22

Regulatory Status

Discontinued

1991

22 Feb

Discontinued Application: 89575

Drug Name

A-METHAPRED

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-02-22

89575 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89575

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-02-22

Regulatory Status

Discontinued

1991

22 Feb

Discontinued Application: 89576

Drug Name

A-METHAPRED

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1991-02-22

89576 / 1 View Details

Active Ingredient

METHYLPREDNISOLONE SODIUM SUCCINATE

Application Number

89576

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1991-02-22

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85447

Drug Name

A-POXIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

85447 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85447

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85447

Drug Name

A-POXIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

85447 / 2 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85447

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85447

Drug Name

A-POXIDE

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85447 / 3 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85447

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85513

Drug Name

A-POXIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85513 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85513

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85517

Drug Name

A-POXIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

85517 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85517

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85518

Drug Name

A-POXIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

85518 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85518

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1994

30 Nov

Discontinued Application: 63265

Drug Name

AMIKACIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1994-11-30

63265 / 1 View Details

Active Ingredient

AMIKACIN SULFATE

Application Number

63265

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1994-11-30

Regulatory Status

Discontinued

1994

31 Oct

Discontinued Application: 63266

Drug Name

AMIKACIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1994-10-31

63266 / 1 View Details

Active Ingredient

AMIKACIN SULFATE

Application Number

63266

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/ML

Approval Date

1994-10-31

Regulatory Status

Discontinued

1984

15 May

Discontinued Application: 18804

Drug Name

AMINOSYN 3.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1984-05-15

18804 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

18804

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1984-05-15

Regulatory Status

Discontinued

1984

08 Aug

Discontinued Application: 18875

Drug Name

AMINOSYN 3.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1984-08-08

18875 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

18875

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1984-08-08

Regulatory Status

Discontinued

1984

15 May

Discontinued Application: 18804

Drug Name

AMINOSYN 3.5% M IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Approval Date

1984-05-15

18804 / 2 View Details

Active Ingredient

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE

Application Number

18804

Product Number

2

Dosage Form

-

Strength

3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Approval Date

1984-05-15

Regulatory Status

Discontinued

1984

08 Aug

Discontinued Application: 18875

Drug Name

AMINOSYN 3.5% M IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Approval Date

1984-08-08

18875 / 2 View Details

Active Ingredient

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE

Application Number

18875

Product Number

2

Dosage Form

-

Strength

3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Approval Date

1984-08-08

Regulatory Status

Discontinued

1984

11 Oct

Discontinued Application: 19118

Drug Name

AMINOSYN 3.5% W/ DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1984-10-11

19118 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19118

Product Number

1

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1984-10-11

Regulatory Status

Discontinued

1984

11 Oct

Discontinued Application: 19120

Drug Name

AMINOSYN 3.5% W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1984-10-11

19120 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19120

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1984-10-11

Regulatory Status

Discontinued

1984

11 Oct

Discontinued Application: 19119

Drug Name

AMINOSYN 4.25% W/ DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1984-10-11

19119 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19119

Product Number

1

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1984-10-11

Regulatory Status

Discontinued

1986

07 Nov

Discontinued Application: 19505

Drug Name

AMINOSYN II 3.5% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1986-11-07

19505 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19505

Product Number

2

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1986-11-07

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 3.5% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1988-09-09

19713 / 6 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

6

Dosage Form

-

Strength

3.5%;25GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1986

07 Nov

Discontinued Application: 19506

Drug Name

AMINOSYN II 3.5% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1986-11-07

19506 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19506

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1986-11-07

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 3.5% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1988-09-09

19713 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

2

Dosage Form

-

Strength

3.5%;5GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1986

10 Oct

Discontinued Application: 19491

Drug Name

AMINOSYN II 3.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1986-10-10

19491 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

19491

Product Number

1

Dosage Form

-

Strength

3.5% (3.5GM/100ML)

Approval Date

1986-10-10

Regulatory Status

Discontinued

1986

16 Dec

Discontinued Application: 19564

Drug Name

AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1986-12-16

19564 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19564

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1986-12-16

Regulatory Status

Discontinued

1988

08 Sep

Discontinued Application: 19712

Drug Name

AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1988-09-08

19712 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19712

Product Number

1

Dosage Form

-

Strength

3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1988-09-08

Regulatory Status

Discontinued

1986

16 Oct

Discontinued Application: 19493

Drug Name

AMINOSYN II 3.5% M IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;32MG/100ML;128MG/100ML;222MG/100ML;49MG/100ML

Approval Date

1986-10-16

19493 / 1 View Details

Active Ingredient

AMINO ACIDS; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19493

Product Number

1

Dosage Form

-

Strength

3.5%;32MG/100ML;128MG/100ML;222MG/100ML;49MG/100ML

Approval Date

1986-10-16

Regulatory Status

Discontinued

1986

16 Dec

Discontinued Application: 19564

Drug Name

AMINOSYN II 3.5% W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

3.5%;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1986-12-16

19564 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19564

Product Number

2

Dosage Form

-

Strength

3.5%;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1986-12-16

Regulatory Status

Discontinued

1988

12 Sep

Discontinued Application: 19714

Drug Name

AMINOSYN II 3.5% W/ ELECTROLYTES IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.5%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

19714 / 1 View Details

Active Ingredient

AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19714

Product Number

1

Dosage Form

-

Strength

3.5%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 4.25% IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

4.25%;10GM/100ML

Approval Date

1988-09-09

19713 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

1

Dosage Form

-

Strength

4.25%;10GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

4.25%;20GM/100ML

Approval Date

1988-09-09

19713 / 4 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

4

Dosage Form

-

Strength

4.25%;20GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1986

07 Nov

Discontinued Application: 19504

Drug Name

AMINOSYN II 4.25% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1986-11-07

19504 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19504

Product Number

2

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1986-11-07

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 4.25% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1988-09-09

19713 / 5 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

5

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1986

16 Dec

Discontinued Application: 19564

Drug Name

AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

4.25%;10GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1986-12-16

19564 / 3 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19564

Product Number

3

Dosage Form

-

Strength

4.25%;10GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML

Approval Date

1986-12-16

Regulatory Status

Discontinued

1988

08 Sep

Discontinued Application: 19712

Drug Name

AMINOSYN II 4.25% W/ ELECT AND ADJUSTED PHOSPHATE IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

4.25%;10GM/100ML;51MG/100ML;176.5MG/100ML;22.4MG/100ML;104.5MG/100ML;205MG/100ML

Approval Date

1988-09-08

19712 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19712

Product Number

2

Dosage Form

-

Strength

4.25%;10GM/100ML;51MG/100ML;176.5MG/100ML;22.4MG/100ML;104.5MG/100ML;205MG/100ML

Approval Date

1988-09-08

Regulatory Status

Discontinued

1988

12 Sep

Discontinued Application: 19714

Drug Name

AMINOSYN II 4.25% W/ ELECTROLYTES IN DEXTROSE 20% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

4.25%;36.8MG/100ML;20GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

19714 / 2 View Details

Active Ingredient

AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19714

Product Number

2

Dosage Form

-

Strength

4.25%;36.8MG/100ML;20GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

Regulatory Status

Discontinued

1986

16 Dec

Discontinued Application: 19564

Drug Name

AMINOSYN II 4.25% W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

4.25%;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1986-12-16

19564 / 4 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19564

Product Number

4

Dosage Form

-

Strength

4.25%;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1986-12-16

Regulatory Status

Discontinued

1988

12 Sep

Discontinued Application: 19714

Drug Name

AMINOSYN II 4.25% W/ ELECTROLYTES IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

4.25%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

19714 / 4 View Details

Active Ingredient

AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19714

Product Number

4

Dosage Form

-

Strength

4.25%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

Regulatory Status

Discontinued

1986

17 Dec

Discontinued Application: 19565

Drug Name

AMINOSYN II 5% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1986-12-17

19565 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19565

Product Number

1

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1986-12-17

Regulatory Status

Discontinued

1988

09 Sep

Discontinued Application: 19713

Drug Name

AMINOSYN II 5% IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1988-09-09

19713 / 3 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

19713

Product Number

3

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1988-09-09

Regulatory Status

Discontinued

1988

12 Sep

Discontinued Application: 19714

Drug Name

AMINOSYN II 5% W/ ELECTROLYTES IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

19714 / 3 View Details

Active Ingredient

AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Application Number

19714

Product Number

3

Dosage Form

-

Strength

5%;36.8MG/100ML;25GM/100ML;51MG/100ML;22.4MG/100ML;261MG/100ML;205MG/100ML

Approval Date

1988-09-12

Regulatory Status

Discontinued

1986

23 Jul

Discontinued Application: 19400

Drug Name

AMINOSYN-HBC 7% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

7% (7GM/100ML)

Approval Date

1986-07-23

19400 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

19400

Product Number

1

Dosage Form

-

Strength

7% (7GM/100ML)

Approval Date

1986-07-23

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83130

Drug Name

AMMONIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

5MEQ/ML

Approval Date

1982-01-01

83130 / 1 View Details

Active Ingredient

AMMONIUM CHLORIDE

Application Number

83130

Product Number

1

Dosage Form

-

Strength

5MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1996

23 Dec

Discontinued Application: 64141

Drug Name

AMPHOTERICIN B

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1996-12-23

64141 / 1 View Details

Active Ingredient

AMPHOTERICIN B

Application Number

64141

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1996-12-23

Regulatory Status

Discontinued

1986

29 Apr

Discontinued Application: 19005

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5%

Product Number

1

Dosage Form

-

Strength

800MG/100ML

Approval Date

1986-04-29

19005 / 1 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19005

Product Number

1

Dosage Form

-

Strength

800MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1986

29 Apr

Discontinued Application: 19005

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5%

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1986-04-29

19005 / 2 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19005

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1986

29 Apr

Discontinued Application: 19005

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5%

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1986-04-29

19005 / 3 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19005

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80001

Drug Name

CALCIUM GLUCEPTATE

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1982-01-01

80001 / 1 View Details

Active Ingredient

CALCIUM GLUCEPTATE

Application Number

80001

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83159

Drug Name

CALCIUM GLUCEPTATE

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1982-01-01

83159 / 1 View Details

Active Ingredient

CALCIUM GLUCEPTATE

Application Number

83159

Product Number

1

Dosage Form

-

Strength

EQ 90MG CALCIUM/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

11 Sep

Discontinued Application: 62547

Drug Name

CEPHALOTHIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1985-09-11

62547 / 1 View Details

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62547

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1985-09-11

Regulatory Status

Discontinued

1985

11 Sep

Discontinued Application: 62547

Drug Name

CEPHALOTHIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1985-09-11

62547 / 2 View Details

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62547

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1985-09-11

Regulatory Status

Discontinued

1985

11 Sep

Discontinued Application: 62548

Drug Name

CEPHALOTHIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1985-09-11

62548 / 1 View Details

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62548

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1985-09-11

Regulatory Status

Discontinued

1985

11 Sep

Discontinued Application: 62548

Drug Name

CEPHALOTHIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1985-09-11

62548 / 2 View Details

Active Ingredient

CEPHALOTHIN SODIUM

Application Number

62548

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1985-09-11

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84411

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

84411 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84411

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84412

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84412 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84412

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84413

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84413 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84413

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84414

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84414 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84414

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84415

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84415 / 1 View Details

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

84415

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87364

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

87364 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

87364

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 87384

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

87384 / 1 View Details

Active Ingredient

CHLORTHALIDONE

Application Number

87384

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2001

29 Jun

Discontinued Application: 65027

Drug Name

CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2001-06-29

65027 / 1 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

65027

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2001-06-29

Regulatory Status

Discontinued

2001

29 Jun

Discontinued Application: 65027

Drug Name

CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

2001-06-29

65027 / 2 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

65027

Product Number

2

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

2001-06-29

Regulatory Status

Discontinued

2001

29 Jun

Discontinued Application: 65027

Drug Name

CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 18MG BASE/ML

Approval Date

2001-06-29

65027 / 3 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

65027

Product Number

3

Dosage Form

-

Strength

EQ 18MG BASE/ML

Approval Date

2001-06-29

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16832

Drug Name

CYLERT

Product Number

1

Dosage Form

-

Strength

18.75MG

Approval Date

1982-01-01

16832 / 1 View Details

Active Ingredient

PEMOLINE

Application Number

16832

Product Number

1

Dosage Form

-

Strength

18.75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16832

Drug Name

CYLERT

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

1982-01-01

16832 / 2 View Details

Active Ingredient

PEMOLINE

Application Number

16832

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16832

Drug Name

CYLERT

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

16832 / 3 View Details

Active Ingredient

PEMOLINE

Application Number

16832

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17703

Drug Name

CYLERT

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1982-01-01

17703 / 1 View Details

Active Ingredient

PEMOLINE

Application Number

17703

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990

11 Jul

Discontinued Application: 19794

Drug Name

DEPAKOTE CP

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1990-07-11

19794 / 1 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

19794

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1990-07-11

Regulatory Status

Discontinued

1990

11 Jul

Discontinued Application: 19794

Drug Name

DEPAKOTE CP

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1990-07-11

19794 / 2 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

19794

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1990-07-11

Regulatory Status

Discontinued

-

Unclassified Application: 20782

Drug Name

DEPAKOTE ER

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

20782 / 1 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

20782

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-

Unclassified Application: 20782

Drug Name

DEPAKOTE ER

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

20782 / 2 View Details

Active Ingredient

DIVALPROEX SODIUM

Application Number

20782

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

Regulatory Status

Unclassified

1982

01 Jan

Discontinued Application: 18055

Drug Name

DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML

Approval Date

1982-01-01

18055 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18055

Product Number

1

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

19 Sep

Discontinued Application: 18923

Drug Name

DEXTROSE 38.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

38.5GM/100ML

Approval Date

1984-09-19

18923 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

18923

Product Number

1

Dosage Form

-

Strength

38.5GM/100ML

Approval Date

1984-09-19

Regulatory Status

Discontinued

1985

04 Oct

Discontinued Application: 19482

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;225MG/100ML

Approval Date

1985-10-04

19482 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19482

Product Number

1

Dosage Form

-

Strength

5GM/100ML;225MG/100ML

Approval Date

1985-10-04

Regulatory Status

Discontinued

1985

04 Oct

Discontinued Application: 19486

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1985-10-04

19486 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19486

Product Number

1

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1985-10-04

Regulatory Status

Discontinued

1985

04 Oct

Discontinued Application: 19484

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1985-10-04

19484 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19484

Product Number

1

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1985-10-04

Regulatory Status

Discontinued

1985

04 Oct

Discontinued Application: 19483

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1985-10-04

19483 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19483

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1985-10-04

Regulatory Status

Discontinued

1989

24 Jan

Discontinued Application: 70656

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1989-01-24

70656 / 1 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70656

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

1989-01-24

Regulatory Status

Discontinued

1989

24 Jan

Discontinued Application: 70657

Drug Name

DOPAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1989-01-24

70657 / 1 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

70657

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

1989-01-24

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 12775

Drug Name

ENDURONYL

Product Number

1

Dosage Form

-

Strength

0.25MG;5MG

Approval Date

1982-01-01

12775 / 1 View Details

Active Ingredient

DESERPIDINE; METHYCLOTHIAZIDE

Application Number

12775

Product Number

1

Dosage Form

-

Strength

0.25MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 12775

Drug Name

ENDURONYL FORTE

Product Number

2

Dosage Form

-

Strength

0.5MG;5MG

Approval Date

1982-01-01

12775 / 2 View Details

Active Ingredient

DESERPIDINE; METHYCLOTHIAZIDE

Application Number

12775

Product Number

2

Dosage Form

-

Strength

0.5MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

08 Sep

Discontinued Application: 70803

Drug Name

ENFLURANE

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

1987-09-08

70803 / 1 View Details

Active Ingredient

ENFLURANE

Application Number

70803

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

1987-09-08

Regulatory Status

Discontinued

1988

04 Jan

Discontinued Application: 62586

Drug Name

ERYTHROCIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-01-04

62586 / 1 View Details

Active Ingredient

ERYTHROMYCIN LACTOBIONATE

Application Number

62586

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1988-01-04

Regulatory Status

Discontinued

1988

04 Jan

Discontinued Application: 62586

Drug Name

ERYTHROCIN

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-01-04

62586 / 2 View Details

Active Ingredient

ERYTHROMYCIN LACTOBIONATE

Application Number

62586

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1988-01-04

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 13448

Drug Name

EUTONYL

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

13448 / 2 View Details

Active Ingredient

PARGYLINE HYDROCHLORIDE

Application Number

13448

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 13448

Drug Name

EUTONYL

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

13448 / 3 View Details

Active Ingredient

PARGYLINE HYDROCHLORIDE

Application Number

13448

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 13448

Drug Name

EUTONYL

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

13448 / 4 View Details

Active Ingredient

PARGYLINE HYDROCHLORIDE

Application Number

13448

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16047

Drug Name

EUTRON

Product Number

1

Dosage Form

-

Strength

5MG;25MG

Approval Date

1982-01-01

16047 / 1 View Details

Active Ingredient

METHYCLOTHIAZIDE; PARGYLINE HYDROCHLORIDE

Application Number

16047

Product Number

1

Dosage Form

-

Strength

5MG;25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990

30 Apr

Discontinued Application: 70636

Drug Name

FENTANYL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/ML

Approval Date

1990-04-30

70636 / 1 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

70636

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/ML

Approval Date

1990-04-30

Regulatory Status

Discontinued

1990

30 Apr

Discontinued Application: 70637

Drug Name

FENTANYL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/ML

Approval Date

1990-04-30

70637 / 1 View Details

Active Ingredient

FENTANYL CITRATE

Application Number

70637

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/ML

Approval Date

1990-04-30

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1983-08-11

62413 / 1 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

1

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 1.4MG BASE/ML

Approval Date

1983-08-11

62413 / 2 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

2

Dosage Form

-

Strength

EQ 1.4MG BASE/ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

3

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1983-08-11

62413 / 3 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

3

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

4

Dosage Form

-

Strength

EQ 1.8MG BASE/ML

Approval Date

1983-08-11

62413 / 4 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

4

Dosage Form

-

Strength

EQ 1.8MG BASE/ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

5

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1983-08-11

62413 / 5 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

5

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

6

Dosage Form

-

Strength

EQ 60MG BASE/100ML

Approval Date

1983-08-11

62413 / 6 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

6

Dosage Form

-

Strength

EQ 60MG BASE/100ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

7

Dosage Form

-

Strength

EQ 70MG BASE/100ML

Approval Date

1983-08-11

62413 / 7 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

7

Dosage Form

-

Strength

EQ 70MG BASE/100ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

8

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1983-08-11

62413 / 8 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

8

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

9

Dosage Form

-

Strength

EQ 90MG BASE/100ML

Approval Date

1983-08-11

62413 / 9 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

9

Dosage Form

-

Strength

EQ 90MG BASE/100ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1983

11 Aug

Discontinued Application: 62413

Drug Name

GENTAMICIN SULFATE

Product Number

10

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1983-08-11

62413 / 10 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62413

Product Number

10

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1983-08-11

Regulatory Status

Discontinued

1987

07 Aug

Discontinued Application: 19057

Drug Name

HYTRIN

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1987-08-07

19057 / 1 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

19057

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

1987-08-07

Regulatory Status

Discontinued

1987

07 Aug

Discontinued Application: 19057

Drug Name

HYTRIN

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1987-08-07

19057 / 2 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

19057

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

1987-08-07

Regulatory Status

Discontinued

1987

07 Aug

Discontinued Application: 19057

Drug Name

HYTRIN

Product Number

3

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-08-07

19057 / 3 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

19057

Product Number

3

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1987-08-07

Regulatory Status

Discontinued

1987

07 Aug

Discontinued Application: 19057

Drug Name

HYTRIN

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1987-08-07

19057 / 4 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

19057

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1987-08-07

Regulatory Status

Discontinued

1994

14 Dec

Discontinued Application: 20347

Drug Name

HYTRIN

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1994-12-14

20347 / 1 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

20347

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1994-12-14

Regulatory Status

Discontinued

1994

14 Dec

Discontinued Application: 20347

Drug Name

HYTRIN

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-14

20347 / 2 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

20347

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-12-14

Regulatory Status

Discontinued

1994

14 Dec

Discontinued Application: 20347

Drug Name

HYTRIN

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1994-12-14

20347 / 3 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

20347

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1994-12-14

Regulatory Status

Discontinued

1994

14 Dec

Discontinued Application: 20347

Drug Name

HYTRIN

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1994-12-14

20347 / 4 View Details

Active Ingredient

TERAZOSIN HYDROCHLORIDE

Application Number

20347

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1994-12-14

Regulatory Status

Discontinued

1989

18 Dec

Discontinued Application: 19784

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

1989-12-18

19784 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

19784

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

1989-12-18

Regulatory Status

Discontinued

1985

14 Jun

Discontinued Application: 70556

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-06-14

70556 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

70556

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-06-14

Regulatory Status

Discontinued

1986

25 Jul

Discontinued Application: 71264

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1986-07-25

71264 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

71264

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1986-07-25

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17895

Drug Name

JANIMINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

17895 / 1 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

17895

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17895

Drug Name

JANIMINE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

17895 / 2 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

17895

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17895

Drug Name

JANIMINE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

17895 / 3 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

17895

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985

24 Oct

Discontinued Application: 19485

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-10-24

19485 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19485

Product Number

1

Dosage Form

-

Strength

20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-10-24

Regulatory Status

Discontinued

1983

02 Feb

Discontinued Application: 87980

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1983-02-02

87980 / 1 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

87980

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1983-02-02

Regulatory Status

Discontinued

1988

25 May

Discontinued Application: 89362

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1988-05-25

89362 / 1 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

89362

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1988-05-25

Regulatory Status

Discontinued

1985

09 Jul

Discontinued Application: 18954

Drug Name

LIDOCAINE HYDROCHLORIDE 0.2% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1985-07-09

18954 / 1 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18954

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1985-07-09

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83154

Drug Name

LIDOCAINE HYDROCHLORIDE W/ EPINEPHRINE

Product Number

1

Dosage Form

-

Strength

0.01MG/ML;1%

Approval Date

1982-01-01

83154 / 1 View Details

Active Ingredient

EPINEPHRINE; LIDOCAINE HYDROCHLORIDE

Application Number

83154

Product Number

1

Dosage Form

-

Strength

0.01MG/ML;1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18203

Drug Name

LIPOSYN 10%

Product Number

1

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1982-01-01

18203 / 1 View Details

Active Ingredient

SAFFLOWER OIL

Application Number

18203

Product Number

1

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18614

Drug Name

LIPOSYN 20%

Product Number

1

Dosage Form

-

Strength

20% (20GM/100ML)

Approval Date

1982-01-01

18614 / 1 View Details

Active Ingredient

SAFFLOWER OIL

Application Number

18614

Product Number

1

Dosage Form

-

Strength

20% (20GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18297

Drug Name

LOPURIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

18297 / 1 View Details

Active Ingredient

ALLOPURINOL

Application Number

18297

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18297

Drug Name

LOPURIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

18297 / 2 View Details

Active Ingredient

ALLOPURINOL

Application Number

18297

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80385

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

80385 / 1 View Details

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

80385

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80386

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

80386 / 1 View Details

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

80386

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80387

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

80387 / 1 View Details

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

80387

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80388

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

80388 / 1 View Details

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

80388

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80389

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG/ML

Approval Date

1982-01-01

80389 / 1 View Details

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

80389

Product Number

1

Dosage Form

-

Strength

75MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997

22 Nov

Discontinued Application: 20632

Drug Name

MERIDIA

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1997-11-22

20632 / 1 View Details

Active Ingredient

SIBUTRAMINE HYDROCHLORIDE

Application Number

20632

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1997-11-22

Regulatory Status

Discontinued

1997

22 Nov

Discontinued Application: 20632

Drug Name

MERIDIA

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1997-11-22

20632 / 2 View Details

Active Ingredient

SIBUTRAMINE HYDROCHLORIDE

Application Number

20632

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1997-11-22

Regulatory Status

Discontinued

1997

22 Nov

Discontinued Application: 20632

Drug Name

MERIDIA

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

1997-11-22

20632 / 3 View Details

Active Ingredient

SIBUTRAMINE HYDROCHLORIDE

Application Number

20632

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

1997-11-22

Regulatory Status

Discontinued

1983

18 Nov

Discontinued Application: 18889

Drug Name

METRONIDAZOLE

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1983-11-18

18889 / 1 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18889

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1983-11-18

Regulatory Status

Discontinued

1989

03 Feb

Discontinued Application: 70917

Drug Name

NALBUPHINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG/ML (20MG/ML)

Approval Date

1989-02-03

70917 / 1 View Details

Active Ingredient

NALBUPHINE HYDROCHLORIDE

Application Number

70917

Product Number

1

Dosage Form

-

Strength

20MG/ML (20MG/ML)

Approval Date

1989-02-03

Regulatory Status

Discontinued

1987

16 Nov

Discontinued Application: 71555

Drug Name

NITROPRESS

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1987-11-16

71555 / 1 View Details

Active Ingredient

SODIUM NITROPRUSSIDE

Application Number

71555

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

1987-11-16

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16814

Drug Name

NORISODRINE AEROTROL

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1982-01-01

16814 / 1 View Details

Active Ingredient

ISOPROTERENOL HYDROCHLORIDE

Application Number

16814

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1996

01 Mar

Discontinued Application: 20680

Drug Name

NORVIR

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1996-03-01

20680 / 1 View Details

Active Ingredient

RITONAVIR

Application Number

20680

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1996-03-01

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19185

Drug Name

OXYTOCIN 10 USP UNITS IN DEXTROSE 5%

Product Number

3

Dosage Form

-

Strength

2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

19185 / 3 View Details

Active Ingredient

OXYTOCIN

Application Number

19185

Product Number

3

Dosage Form

-

Strength

2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19185

Drug Name

OXYTOCIN 10 USP UNITS IN DEXTROSE 5%

Product Number

4

Dosage Form

-

Strength

1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

19185 / 4 View Details

Active Ingredient

OXYTOCIN

Application Number

19185

Product Number

4

Dosage Form

-

Strength

1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19185

Drug Name

OXYTOCIN 20 USP UNITS IN DEXTROSE 5%

Product Number

2

Dosage Form

-

Strength

2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

19185 / 2 View Details

Active Ingredient

OXYTOCIN

Application Number

19185

Product Number

2

Dosage Form

-

Strength

2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19185

Drug Name

OXYTOCIN 5 USP UNITS IN DEXTROSE 5%

Product Number

1

Dosage Form

-

Strength

1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

19185 / 1 View Details

Active Ingredient

OXYTOCIN

Application Number

19185

Product Number

1

Dosage Form

-

Strength

1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17020

Drug Name

PANWARFIN

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

17020 / 1 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

17020

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17020

Drug Name

PANWARFIN

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

17020 / 2 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

17020

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17020

Drug Name

PANWARFIN

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

17020 / 3 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

17020

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17020

Drug Name

PANWARFIN

Product Number

4

Dosage Form

-

Strength

7.5MG

Approval Date

1982-01-01

17020 / 4 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

17020

Product Number

4

Dosage Form

-

Strength

7.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17020

Drug Name

PANWARFIN

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

17020 / 5 View Details

Active Ingredient

WARFARIN SODIUM

Application Number

17020

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

31 Jul

Discontinued Application: 88572

Drug Name

PEDIATRIC LTA KIT

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1984-07-31

88572 / 1 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

88572

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1984-07-31

Regulatory Status

Discontinued

-

Unclassified Application: 13056

Drug Name

PENTHRANE

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

-

13056 / 1 View Details

Active Ingredient

METHOXYFLURANE

Application Number

13056

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

-

Regulatory Status

Unclassified

1982

01 Jan

Discontinued Application: 11679

Drug Name

PENTOTHAL

Product Number

1

Dosage Form

-

Strength

400MG/GM

Approval Date

1982-01-01

11679 / 1 View Details

Active Ingredient

THIOPENTAL SODIUM

Application Number

11679

Product Number

1

Dosage Form

-

Strength

400MG/GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84160

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1982-01-01

84160 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

84160

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84166

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84166 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

84166

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84222

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

84222 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

84222

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84223

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

84223 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

84223

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84539

Drug Name

PROMETHAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

84539 / 1 View Details

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

84539

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 84075

Drug Name

PROPYLTHIOURACIL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

84075 / 1 View Details

Active Ingredient

PROPYLTHIOURACIL

Application Number

84075

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990

26 Dec

Discontinued Application: 19080

Drug Name

PROSOM

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1990-12-26

19080 / 1 View Details

Active Ingredient

ESTAZOLAM

Application Number

19080

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1990-12-26

Regulatory Status

Discontinued

1990

26 Dec

Discontinued Application: 19080

Drug Name

PROSOM

Product Number

2

Dosage Form

-

Strength

2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-26

19080 / 2 View Details

Active Ingredient

ESTAZOLAM

Application Number

19080

Product Number

2

Dosage Form

-

Strength

2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18462

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

33MG/100ML;30MG/100ML;860MG/100ML

Approval Date

1982-01-01

18462 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18462

Product Number

1

Dosage Form

-

Strength

33MG/100ML;30MG/100ML;860MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

03 Jun

Discontinued Application: 19443

Drug Name

SODIUM BICARBONATE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

44.6MEQ/50ML (0.9MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-06-03

19443 / 1 View Details

Active Ingredient

SODIUM BICARBONATE

Application Number

19443

Product Number

1

Dosage Form

-

Strength

44.6MEQ/50ML (0.9MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-06-03

Regulatory Status

Discontinued

1986

03 Jun

Discontinued Application: 19443

Drug Name

SODIUM BICARBONATE IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

50MEQ/50ML (1MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-06-03

19443 / 2 View Details

Active Ingredient

SODIUM BICARBONATE

Application Number

19443

Product Number

2

Dosage Form

-

Strength

50MEQ/50ML (1MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-06-03

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17013

Drug Name

SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

17013 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

17013

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

13 Jul

Discontinued Application: 19218

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

1984-07-13

19218 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19218

Product Number

1

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

1984-07-13

Regulatory Status

Discontinued

1985

30 Apr

Discontinued Application: 19218

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

180MG/20ML (9MG/ML)

Approval Date

1985-04-30

19218 / 2 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19218

Product Number

2

Dosage Form

-

Strength

180MG/20ML (9MG/ML)

Approval Date

1985-04-30

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61802

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

61802 / 1 View Details

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61802

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61802

Drug Name

TETRACYCLINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

61802 / 2 View Details

Active Ingredient

TETRACYCLINE HYDROCHLORIDE

Application Number

61802

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17638

Drug Name

THYPINONE

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

17638 / 1 View Details

Active Ingredient

PROTIRELIN

Application Number

17638

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

16 Jun

Discontinued Application: 19399

Drug Name

TPN ELECTROLYTES IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

16.5MG/ML;25.4MG/ML;74.6MG/ML;121MG/ML;16.1MG/ML

Approval Date

1986-06-16

19399 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

19399

Product Number

1

Dosage Form

-

Strength

16.5MG/ML;25.4MG/ML;74.6MG/ML;121MG/ML;16.1MG/ML

Approval Date

1986-06-16

Regulatory Status

Discontinued

-

Unclassified Application: 12828

Drug Name

TRAVASE

Product Number

1

Dosage Form

-

Strength

82,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**

Approval Date

-

12828 / 1 View Details

Active Ingredient

SUTILAINS

Application Number

12828

Product Number

1

Dosage Form

-

Strength

82,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**

Approval Date

-

Regulatory Status

Unclassified

1982

01 Jan

Discontinued Application: 16245

Drug Name

VERCYTE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

16245 / 1 View Details

Active Ingredient

PIPOBROMAN

Application Number

16245

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16245

Drug Name

VERCYTE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

16245 / 2 View Details

Active Ingredient

PIPOBROMAN

Application Number

16245

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85667

Drug Name

VICODIN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-01-01

85667 / 1 View Details

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

85667

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983

14 Sep

Discontinued Application: 86333

Drug Name

VICOPRIN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1983-09-14

86333 / 1 View Details

Active Ingredient

ASPIRIN; HYDROCODONE BITARTRATE

Application Number

86333

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1983-09-14

Regulatory Status

Discontinued

Abbott Laboratories
FDA Approved Drugs

Company Overview

Company Snapshot

FDA Approved Drug Records ( 176 records )

Related Databases

Drug Status Breakdown

Official Source

FDA Approved Drug Record Details Preview

Create a New Buying Request

Abbott Laboratories FDA Approved Drugs