Baxter Healthcare Corporation RX

2021

17 Sep

RX Application: 214331

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2021-09-17

214331 / 1 View Details

Active Ingredient

ACETAMINOPHEN

Application Number

214331

Product Number

1

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2021-09-17

Regulatory Status

RX

2025

21 May

RX Application: 214331

Drug Name

ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

650MG/65ML (10MG/ML)

Approval Date

2025-05-21

214331 / 2 View Details

Active Ingredient

ACETAMINOPHEN

Application Number

214331

Product Number

2

Dosage Form

-

Strength

650MG/65ML (10MG/ML)

Approval Date

2025-05-21

Regulatory Status

RX

1982

19 Feb

RX Application: 18523

Drug Name

ACETIC ACID 0.25% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

250MG/100ML

Approval Date

1982-02-19

18523 / 1 View Details

Active Ingredient

ACETIC ACID, GLACIAL

Application Number

18523

Product Number

1

Dosage Form

-

Strength

250MG/100ML

Approval Date

1982-02-19

Regulatory Status

RX

1982

01 Jan

RX Application: 17865

Drug Name

AMINOACETIC ACID 1.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

1.5GM/100ML

Approval Date

1982-01-01

17865 / 1 View Details

Active Ingredient

GLYCINE

Application Number

17865

Product Number

1

Dosage Form

-

Strength

1.5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1989

26 Oct

RX Application: 50640

Drug Name

BACTOCILL IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1989-10-26

50640 / 2 View Details

Active Ingredient

OXACILLIN SODIUM

Application Number

50640

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1989-10-26

Regulatory Status

RX

2022

15 Dec

RX Application: 216078

Drug Name

BENDAMUSTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/4ML (25MG/ML)

Approval Date

2022-12-15

216078 / 1 View Details

Active Ingredient

BENDAMUSTINE HYDROCHLORIDE

Application Number

216078

Product Number

1

Dosage Form

-

Strength

100MG/4ML (25MG/ML)

Approval Date

2022-12-15

Regulatory Status

RX

2003

25 Feb

RX Application: 19386

Drug Name

BREVIBLOC

Product Number

6

Dosage Form

-

Strength

10MG/ML

Approval Date

2003-02-25

19386 / 6 View Details

Active Ingredient

ESMOLOL HYDROCHLORIDE

Application Number

19386

Product Number

6

Dosage Form

-

Strength

10MG/ML

Approval Date

2003-02-25

Regulatory Status

RX

2003

27 Jan

RX Application: 19386

Drug Name

BREVIBLOC DOUBLE STRENGTH IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

2GM/100ML

Approval Date

2003-01-27

19386 / 5 View Details

Active Ingredient

ESMOLOL HYDROCHLORIDE

Application Number

19386

Product Number

5

Dosage Form

-

Strength

2GM/100ML

Approval Date

2003-01-27

Regulatory Status

RX

2001

16 Feb

RX Application: 19386

Drug Name

BREVIBLOC IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

1GM/100ML

Approval Date

2001-02-16

19386 / 4 View Details

Active Ingredient

ESMOLOL HYDROCHLORIDE

Application Number

19386

Product Number

4

Dosage Form

-

Strength

1GM/100ML

Approval Date

2001-02-16

Regulatory Status

RX

2000

21 Apr

RX Application: 75323

Drug Name

CARDIOPLEGIC IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

17.6MG/100ML;325.3MG/100ML;119.3MG/100ML;643MG/100ML

Approval Date

2000-04-21

75323 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

75323

Product Number

1

Dosage Form

-

Strength

17.6MG/100ML;325.3MG/100ML;119.3MG/100ML;643MG/100ML

Approval Date

2000-04-21

Regulatory Status

RX

2015

07 Aug

RX Application: 207131

Drug Name

CEFAZOLIN IN DEXTROSE

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

Approval Date

2015-08-07

207131 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

207131

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

Approval Date

2015-08-07

Regulatory Status

RX

2021

01 Feb

RX Application: 207131

Drug Name

CEFAZOLIN IN DEXTROSE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

Approval Date

2021-02-01

207131 / 2 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

207131

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

Approval Date

2021-02-01

Regulatory Status

RX

2024

31 May

RX Application: 207131

Drug Name

CEFAZOLIN IN DEXTROSE

Product Number

3

Dosage Form

-

Strength

EQ 3GM BASE/150ML (EQ 20MG BASE/ML)

Approval Date

2024-05-31

207131 / 3 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

207131

Product Number

3

Dosage Form

-

Strength

EQ 3GM BASE/150ML (EQ 20MG BASE/ML)

Approval Date

2024-05-31

Regulatory Status

RX

2008

05 Aug

RX Application: 50817

Drug Name

CEFEPIME IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

Approval Date

2008-08-05

50817 / 1 View Details

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

50817

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

Approval Date

2008-08-05

Regulatory Status

RX

2008

05 Aug

RX Application: 50817

Drug Name

CEFEPIME IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

Approval Date

2008-08-05

50817 / 2 View Details

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

50817

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

Approval Date

2008-08-05

Regulatory Status

RX

2005

23 Aug

RX Application: 65224

Drug Name

CEFTRIAXONE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

2005-08-23

65224 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65224

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

2005-08-23

Regulatory Status

RX

2005

23 Aug

RX Application: 65224

Drug Name

CEFTRIAXONE IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

2005-08-23

65224 / 2 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65224

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

2005-08-23

Regulatory Status

RX

2017

20 Apr

RX Application: 208083

Drug Name

CLINDAMYCIN PHOSPHATE IN 0.9% SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE/50ML (EQ 6MG BASE/ML)

Approval Date

2017-04-20

208083 / 1 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208083

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE/50ML (EQ 6MG BASE/ML)

Approval Date

2017-04-20

Regulatory Status

RX

2017

20 Apr

RX Application: 208083

Drug Name

CLINDAMYCIN PHOSPHATE IN 0.9% SODIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 600MG BASE/50ML (EQ 12MG BASE/ML)

Approval Date

2017-04-20

208083 / 2 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208083

Product Number

2

Dosage Form

-

Strength

EQ 600MG BASE/50ML (EQ 12MG BASE/ML)

Approval Date

2017-04-20

Regulatory Status

RX

2017

20 Apr

RX Application: 208083

Drug Name

CLINDAMYCIN PHOSPHATE IN 0.9% SODIUM CHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 900MG BASE/50ML (EQ 18MG BASE/ML)

Approval Date

2017-04-20

208083 / 3 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208083

Product Number

3

Dosage Form

-

Strength

EQ 900MG BASE/50ML (EQ 18MG BASE/ML)

Approval Date

2017-04-20

Regulatory Status

RX

2017

28 Jun

RX Application: 208084

Drug Name

CLINDAMYCIN PHOSPHATE IN 5% DEXTROSE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2017-06-28

208084 / 1 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208084

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2017-06-28

Regulatory Status

RX

2017

28 Jun

RX Application: 208084

Drug Name

CLINDAMYCIN PHOSPHATE IN 5% DEXTROSE IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

2017-06-28

208084 / 2 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208084

Product Number

2

Dosage Form

-

Strength

EQ 12MG BASE/ML

Approval Date

2017-06-28

Regulatory Status

RX

2017

28 Jun

RX Application: 208084

Drug Name

CLINDAMYCIN PHOSPHATE IN 5% DEXTROSE IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 18MG BASE/ML

Approval Date

2017-06-28

208084 / 3 View Details

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

208084

Product Number

3

Dosage Form

-

Strength

EQ 18MG BASE/ML

Approval Date

2017-06-28

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 2.75/10 SULFITE FREE IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

2.75%;10GM/100ML

Approval Date

1997-09-29

20734 / 2 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

2

Dosage Form

-

Strength

2.75%;10GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 2.75/25 SULFITE FREE IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

2.75%;25GM/100ML

Approval Date

1997-09-29

20734 / 5 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

5

Dosage Form

-

Strength

2.75%;25GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 2.75/5 SULFITE FREE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.75%;5GM/100ML

Approval Date

1997-09-29

20734 / 1 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

1

Dosage Form

-

Strength

2.75%;5GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 4.25/10 SULFITE FREE IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

4.25%;10GM/100ML

Approval Date

1997-09-29

20734 / 8 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

8

Dosage Form

-

Strength

4.25%;10GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 4.25/20 SULFITE FREE IN DEXTROSE 20% IN PLASTIC CONTAINER

Product Number

10

Dosage Form

-

Strength

4.25%;20GM/100ML

Approval Date

1997-09-29

20734 / 10 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

10

Dosage Form

-

Strength

4.25%;20GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 4.25/25 SULFITE FREE IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1997-09-29

20734 / 11 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

11

Dosage Form

-

Strength

4.25%;25GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 4.25/5 SULFITE FREE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

4.25%;5GM/100ML

Approval Date

1997-09-29

20734 / 7 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

7

Dosage Form

-

Strength

4.25%;5GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 5/10 SULFITE FREE IN DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

14

Dosage Form

-

Strength

5%;10GM/100ML

Approval Date

1997-09-29

20734 / 14 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

14

Dosage Form

-

Strength

5%;10GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 5/15 SULFITE FREE IN DEXTROSE 15% IN PLASTIC CONTAINER

Product Number

15

Dosage Form

-

Strength

5%;15GM/100ML

Approval Date

1997-09-29

20734 / 15 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

15

Dosage Form

-

Strength

5%;15GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 5/20 SULFITE FREE IN DEXTROSE 20% IN PLASTIC CONTAINER

Product Number

16

Dosage Form

-

Strength

5%;20GM/100ML

Approval Date

1997-09-29

20734 / 16 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

16

Dosage Form

-

Strength

5%;20GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 5/25 SULFITE FREE IN DEXTROSE 25% IN PLASTIC CONTAINER

Product Number

17

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1997-09-29

20734 / 17 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

17

Dosage Form

-

Strength

5%;25GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

1997

29 Sep

RX Application: 20734

Drug Name

CLINIMIX 5/35 SULFITE FREE IN DEXTROSE 35% IN PLASTIC CONTAINER

Product Number

18

Dosage Form

-

Strength

5%;35GM/100ML

Approval Date

1997-09-29

20734 / 18 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

18

Dosage Form

-

Strength

5%;35GM/100ML

Approval Date

1997-09-29

Regulatory Status

RX

2021

13 Apr

RX Application: 20734

Drug Name

CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER

Product Number

19

Dosage Form

-

Strength

8%;14GM/100ML

Approval Date

2021-04-13

20734 / 19 View Details

Active Ingredient

AMINO ACIDS; DEXTROSE

Application Number

20734

Product Number

19

Dosage Form

-

Strength

8%;14GM/100ML

Approval Date

2021-04-13

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 2.75/10 SULFITE FREE W/ ELECT IN DEXTROSE 10% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

2.75%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

20678 / 2 View Details

Active Ingredient

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

Application Number

20678

Product Number

2

Dosage Form

-

Strength

2.75%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 2.75/25 SULFITE FREE W/ ELECT IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

2.75%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

20678 / 5 View Details

Active Ingredient

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

Application Number

20678

Product Number

5

Dosage Form

-

Strength

2.75%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 2.75/5 SULFITE FREE W/ ELECT IN DEXTROSE 5% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.75%;33MG/100ML;5GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

20678 / 1 View Details

Active Ingredient

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

Application Number

20678

Product Number

1

Dosage Form

-

Strength

2.75%;33MG/100ML;5GM/100ML;51MG/100ML;261MG/100ML;217MG/100ML;112MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 4.25/10 SULFITE FREE W/ ELECT IN DEXTROSE 10% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

4.25%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

20678 / 9 View Details

Active Ingredient

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

Application Number

20678

Product Number

9

Dosage Form

-

Strength

4.25%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 4.25/20 SULFITE FREE W/ ELECT IN DEXTROSE 20% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

4.25%;33MG/100ML;20GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

20678 / 11 View Details

Active Ingredient

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

Application Number

20678

Product Number

11

Dosage Form

-

Strength

4.25%;33MG/100ML;20GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 4.25/25 SULFITE FREE W/ ELECT IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

12

Dosage Form

-

Strength

4.25%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

20678 / 12 View Details

Active Ingredient

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

Application Number

20678

Product Number

12

Dosage Form

-

Strength

4.25%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 4.25/5 SULFITE FREE W/ ELECT IN DEXTROSE 5% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

4.25%;33MG/100ML;5GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

20678 / 8 View Details

Active Ingredient

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

Application Number

20678

Product Number

8

Dosage Form

-

Strength

4.25%;33MG/100ML;5GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 5/10 SULFITE FREE W/ ELECT IN DEXTROSE 10% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

16

Dosage Form

-

Strength

5%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

20678 / 16 View Details

Active Ingredient

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

Application Number

20678

Product Number

16

Dosage Form

-

Strength

5%;33MG/100ML;10GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 5/15 SULFITE FREE W/ ELECT IN DEXTROSE 15% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

17

Dosage Form

-

Strength

5%;33MG/100ML;15GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

20678 / 17 View Details

Active Ingredient

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

Application Number

20678

Product Number

17

Dosage Form

-

Strength

5%;33MG/100ML;15GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 5/20 SULFITE FREE W/ ELECT IN 20% DEXTROSE W/ CALCIUM IN PLASTIC CONTAINER

Product Number

18

Dosage Form

-

Strength

5%;33MG/100ML;20GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

20678 / 18 View Details

Active Ingredient

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

Application Number

20678

Product Number

18

Dosage Form

-

Strength

5%;33MG/100ML;20GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 5/25 SULFITE FREE W/ ELECT IN DEXTROSE 25% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

19

Dosage Form

-

Strength

5%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

20678 / 19 View Details

Active Ingredient

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

Application Number

20678

Product Number

19

Dosage Form

-

Strength

5%;33MG/100ML;25GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1997

26 Mar

RX Application: 20678

Drug Name

CLINIMIX E 5/35 SULFITE FREE W/ ELECT IN DEXTROSE 35% W/ CALCIUM IN PLASTIC CONTAINER

Product Number

21

Dosage Form

-

Strength

5%;33MG/100ML;35GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

20678 / 21 View Details

Active Ingredient

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

Application Number

20678

Product Number

21

Dosage Form

-

Strength

5%;33MG/100ML;35GM/100ML;51MG/100ML;261MG/100ML;340MG/100ML;59MG/100ML

Approval Date

1997-03-26

Regulatory Status

RX

1996

30 Aug

RX Application: 20512

Drug Name

CLINISOL 15% SULFITE FREE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

15% (15GM/100ML)

Approval Date

1996-08-30

20512 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

20512

Product Number

1

Dosage Form

-

Strength

15% (15GM/100ML)

Approval Date

1996-08-30

Regulatory Status

RX

2013

03 Oct

RX Application: 204508

Drug Name

CLINOLIPID 20%

Product Number

1

Dosage Form

-

Strength

16%(160GM/1000ML);4% (40GM/1000ML)

Approval Date

2013-10-03

204508 / 1 View Details

Active Ingredient

OLIVE OIL; SOYBEAN OIL

Application Number

204508

Product Number

1

Dosage Form

-

Strength

16%(160GM/1000ML);4% (40GM/1000ML)

Approval Date

2013-10-03

Regulatory Status

RX

2008

21 May

RX Application: 40745

Drug Name

CYCLOPHOSPHAMIDE

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2008-05-21

40745 / 1 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

40745

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2008-05-21

Regulatory Status

RX

2008

21 May

RX Application: 40745

Drug Name

CYCLOPHOSPHAMIDE

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2008-05-21

40745 / 2 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

40745

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2008-05-21

Regulatory Status

RX

2008

21 May

RX Application: 40745

Drug Name

CYCLOPHOSPHAMIDE

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

2008-05-21

40745 / 3 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

40745

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

2008-05-21

Regulatory Status

RX

2023

28 Jun

RX Application: 217651

Drug Name

CYCLOPHOSPHAMIDE

Product Number

1

Dosage Form

-

Strength

500MG/2.5ML (200MG/ML)

Approval Date

2023-06-28

217651 / 1 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

217651

Product Number

1

Dosage Form

-

Strength

500MG/2.5ML (200MG/ML)

Approval Date

2023-06-28

Regulatory Status

RX

2023

28 Jun

RX Application: 217651

Drug Name

CYCLOPHOSPHAMIDE

Product Number

2

Dosage Form

-

Strength

1GM/5ML (200MG/ML)

Approval Date

2023-06-28

217651 / 2 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

217651

Product Number

2

Dosage Form

-

Strength

1GM/5ML (200MG/ML)

Approval Date

2023-06-28

Regulatory Status

RX

1982

01 Jan

RX Application: 12141

Drug Name

CYTOXAN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

12141 / 1 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

12141

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 12141

Drug Name

CYTOXAN

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

12141 / 2 View Details

Active Ingredient

CYCLOPHOSPHAMIDE

Application Number

12141

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

RX

2023

27 Feb

RX Application: 213645

Drug Name

DAPTOMYCIN IN 0.9% SODIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

350MG/50ML (7MG/ML)

Approval Date

2023-02-27

213645 / 2 View Details

Active Ingredient

DAPTOMYCIN

Application Number

213645

Product Number

2

Dosage Form

-

Strength

350MG/50ML (7MG/ML)

Approval Date

2023-02-27

Regulatory Status

RX

2023

27 Feb

RX Application: 213645

Drug Name

DAPTOMYCIN IN 0.9% SODIUM CHLORIDE

Product Number

3

Dosage Form

-

Strength

500MG/50ML (10MG/ML)

Approval Date

2023-02-27

213645 / 3 View Details

Active Ingredient

DAPTOMYCIN

Application Number

213645

Product Number

3

Dosage Form

-

Strength

500MG/50ML (10MG/ML)

Approval Date

2023-02-27

Regulatory Status

RX

2023

27 Feb

RX Application: 213645

Drug Name

DAPTOMYCIN IN 0.9% SODIUM CHLORIDE

Product Number

4

Dosage Form

-

Strength

700MG/100ML (7MG/ML)

Approval Date

2023-02-27

213645 / 4 View Details

Active Ingredient

DAPTOMYCIN

Application Number

213645

Product Number

4

Dosage Form

-

Strength

700MG/100ML (7MG/ML)

Approval Date

2023-02-27

Regulatory Status

RX

2023

27 Feb

RX Application: 213645

Drug Name

DAPTOMYCIN IN 0.9% SODIUM CHLORIDE

Product Number

5

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2023-02-27

213645 / 5 View Details

Active Ingredient

DAPTOMYCIN

Application Number

213645

Product Number

5

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2023-02-27

Regulatory Status

RX

2026

15 Apr

RX Application: 208103

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/2ML (EQ 100MCG BASE/ML)

Approval Date

2026-04-15

208103 / 1 View Details

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

208103

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/2ML (EQ 100MCG BASE/ML)

Approval Date

2026-04-15

Regulatory Status

RX

2018

21 Aug

RX Application: 208532

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)

Approval Date

2018-08-21

208532 / 1 View Details

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

208532

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)

Approval Date

2018-08-21

Regulatory Status

RX

2018

21 Aug

RX Application: 208532

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)

Approval Date

2018-08-21

208532 / 2 View Details

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

208532

Product Number

2

Dosage Form

-

Strength

EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)

Approval Date

2018-08-21

Regulatory Status

RX

1982

01 Jan

RX Application: 16694

Drug Name

DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

16694 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

16694

Product Number

1

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16697

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;450MG/100ML

Approval Date

1982-01-01

16697 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

16697

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17484

Drug Name

DEXTROSE 5% AND ELECTROLYTE NO. 48 IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;141MG/100ML;20MG/100ML;12MG/100ML;260MG/100ML

Approval Date

1982-01-01

17484 / 1 View Details

Active Ingredient

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

17484

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;141MG/100ML;20MG/100ML;12MG/100ML;260MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17634

Drug Name

DEXTROSE 5% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1982-01-01

17634 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

17634

Product Number

4

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17634

Drug Name

DEXTROSE 5% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1982-01-01

17634 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

17634

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17634

Drug Name

DEXTROSE 5% AND POTASSIUM CHLORIDE 0.224% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;224MG/100ML

Approval Date

1982-01-01

17634 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

17634

Product Number

3

Dosage Form

-

Strength

5GM/100ML;224MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17634

Drug Name

DEXTROSE 5% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1982-01-01

17634 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

17634

Product Number

2

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16673

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16673 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

16673

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1985

30 Oct

RX Application: 16673

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

50MG/ML

Approval Date

1985-10-30

16673 / 3 View Details

Active Ingredient

DEXTROSE

Application Number

16673

Product Number

3

Dosage Form

-

Strength

50MG/ML

Approval Date

1985-10-30

Regulatory Status

RX

1992

07 Dec

RX Application: 20179

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1992-12-07

20179 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

20179

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1992-12-07

Regulatory Status

RX

1992

07 Dec

RX Application: 20179

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1992-12-07

20179 / 2 View Details

Active Ingredient

DEXTROSE

Application Number

20179

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1992-12-07

Regulatory Status

RX

1982

01 Jan

RX Application: 16689

Drug Name

DEXTROSE 5% IN SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1982-01-01

16689 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

16689

Product Number

1

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16687

Drug Name

DEXTROSE 5% IN SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1982-01-01

16687 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

16687

Product Number

1

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16683

Drug Name

DEXTROSE 5% IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1982-01-01

16683 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

16683

Product Number

1

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16678

Drug Name

DEXTROSE 5% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1982-01-01

16678 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

16678

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

13 Apr

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 10MEQ

Product Number

6

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1982-04-13

18037 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

6

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1982-04-13

Regulatory Status

RX

1982

13 Apr

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 10MEQ

Product Number

7

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-04-13

18037 / 7 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

7

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-04-13

Regulatory Status

RX

1982

01 Jan

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 15MEQ (K)

Product Number

4

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;200MG/100ML

Approval Date

1982-01-01

18037 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

4

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

13 Apr

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 20MEQ

Product Number

8

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-04-13

18037 / 8 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

8

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-04-13

Regulatory Status

RX

1982

01 Jan

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 20MEQ (K)

Product Number

1

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1982-01-01

18037 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

1

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

13 Apr

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 30MEQ

Product Number

5

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;200MG/100ML

Approval Date

1982-04-13

18037 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

5

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;200MG/100ML

Approval Date

1982-04-13

Regulatory Status

RX

1982

13 Apr

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 40MEQ

Product Number

9

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1982-04-13

18037 / 9 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

9

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1982-04-13

Regulatory Status

RX

1982

01 Jan

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 5MEQ

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1982-01-01

18037 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 18037

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 5MEQ (K)

Product Number

3

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-01-01

18037 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18037

Product Number

3

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

5

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 15MEQ IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

3

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 30MEQ IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 7 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

7

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 8 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

8

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

23 Mar

RX Application: 18629

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 5MEQ IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;330MG/100ML

Approval Date

1982-03-23

18629 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18629

Product Number

1

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;330MG/100ML

Approval Date

1982-03-23

Regulatory Status

RX

1982

01 Jan

RX Application: 18008

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 20MEQ (K) IN PLASTIC CONTAINER

Product Number

10

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1982-01-01

18008 / 10 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

10

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1991

02 Jul

RX Application: 20047

Drug Name

DEXTROSE 50% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

50GM/100ML

Approval Date

1991-07-02

20047 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

20047

Product Number

1

Dosage Form

-

Strength

50GM/100ML

Approval Date

1991-07-02

Regulatory Status

RX

1991

02 Jul

RX Application: 20047

Drug Name

DEXTROSE 70% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

70GM/100ML

Approval Date

1991-07-02

20047 / 3 View Details

Active Ingredient

DEXTROSE

Application Number

20047

Product Number

3

Dosage Form

-

Strength

70GM/100ML

Approval Date

1991-07-02

Regulatory Status

RX

2026

28 Jul

RX Application: 219882

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG/2ML (5MG/ML)

Approval Date

2026-07-28

219882 / 1 View Details

Active Ingredient

DIAZEPAM

Application Number

219882

Product Number

1

Dosage Form

-

Strength

10MG/2ML (5MG/ML)

Approval Date

2026-07-28

Regulatory Status

RX

2026

28 Jul

RX Application: 219882

Drug Name

DIAZEPAM

Product Number

2

Dosage Form

-

Strength

20MG/4ML (5MG/ML)

Approval Date

2026-07-28

219882 / 2 View Details

Active Ingredient

DIAZEPAM

Application Number

219882

Product Number

2

Dosage Form

-

Strength

20MG/4ML (5MG/ML)

Approval Date

2026-07-28

Regulatory Status

RX

1993

19 Oct

RX Application: 20255

Drug Name

DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/100ML

Approval Date

1993-10-19

20255 / 1 View Details

Active Ingredient

DOBUTAMINE HYDROCHLORIDE

Application Number

20255

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/100ML

Approval Date

1993-10-19

Regulatory Status

RX

1993

19 Oct

RX Application: 20255

Drug Name

DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1993-10-19

20255 / 3 View Details

Active Ingredient

DOBUTAMINE HYDROCHLORIDE

Application Number

20255

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1993-10-19

Regulatory Status

RX

1993

19 Oct

RX Application: 20255

Drug Name

DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

EQ 200MG BASE/100ML

Approval Date

1993-10-19

20255 / 4 View Details

Active Ingredient

DOBUTAMINE HYDROCHLORIDE

Application Number

20255

Product Number

4

Dosage Form

-

Strength

EQ 200MG BASE/100ML

Approval Date

1993-10-19

Regulatory Status

RX

1993

19 Oct

RX Application: 20255

Drug Name

DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

EQ 400MG BASE/100ML

Approval Date

1993-10-19

20255 / 5 View Details

Active Ingredient

DOBUTAMINE HYDROCHLORIDE

Application Number

20255

Product Number

5

Dosage Form

-

Strength

EQ 400MG BASE/100ML

Approval Date

1993-10-19

Regulatory Status

RX

1987

27 Mar

RX Application: 19615

Drug Name

DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

80MG/100ML

Approval Date

1987-03-27

19615 / 1 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19615

Product Number

1

Dosage Form

-

Strength

80MG/100ML

Approval Date

1987-03-27

Regulatory Status

RX

1987

27 Mar

RX Application: 19615

Drug Name

DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

160MG/100ML

Approval Date

1987-03-27

19615 / 2 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19615

Product Number

2

Dosage Form

-

Strength

160MG/100ML

Approval Date

1987-03-27

Regulatory Status

RX

1987

27 Mar

RX Application: 19615

Drug Name

DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

320MG/100ML

Approval Date

1987-03-27

19615 / 3 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19615

Product Number

3

Dosage Form

-

Strength

320MG/100ML

Approval Date

1987-03-27

Regulatory Status

RX

1987

27 Mar

RX Application: 19615

Drug Name

DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

640MG/100ML

Approval Date

1987-03-27

19615 / 4 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19615

Product Number

4

Dosage Form

-

Strength

640MG/100ML

Approval Date

1987-03-27

Regulatory Status

RX

1995

17 Nov

RX Application: 50718

Drug Name

DOXIL (LIPOSOMAL)

Product Number

1

Dosage Form

-

Strength

20MG/10ML (2MG/ML)

Approval Date

1995-11-17

50718 / 1 View Details

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

50718

Product Number

1

Dosage Form

-

Strength

20MG/10ML (2MG/ML)

Approval Date

1995-11-17

Regulatory Status

RX

2000

13 Jun

RX Application: 50718

Drug Name

DOXIL (LIPOSOMAL)

Product Number

2

Dosage Form

-

Strength

50MG/25ML (2MG/ML)

Approval Date

2000-06-13

50718 / 2 View Details

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

50718

Product Number

2

Dosage Form

-

Strength

50MG/25ML (2MG/ML)

Approval Date

2000-06-13

Regulatory Status

RX

2022

19 Oct

RX Application: 212219

Drug Name

DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL)

Product Number

1

Dosage Form

-

Strength

20MG/10ML (2MG/ML)

Approval Date

2022-10-19

212219 / 1 View Details

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

212219

Product Number

1

Dosage Form

-

Strength

20MG/10ML (2MG/ML)

Approval Date

2022-10-19

Regulatory Status

RX

2022

19 Oct

RX Application: 212219

Drug Name

DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL)

Product Number

2

Dosage Form

-

Strength

50MG/25ML (2MG/ML)

Approval Date

2022-10-19

212219 / 2 View Details

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

212219

Product Number

2

Dosage Form

-

Strength

50MG/25ML (2MG/ML)

Approval Date

2022-10-19

Regulatory Status

RX

2026

08 Jul

RX Application: 216740

Drug Name

EPHEDRINE SULFATE

Product Number

1

Dosage Form

-

Strength

50MG/ML (50MG/ML)

Approval Date

2026-07-08

216740 / 1 View Details

Active Ingredient

EPHEDRINE SULFATE

Application Number

216740

Product Number

1

Dosage Form

-

Strength

50MG/ML (50MG/ML)

Approval Date

2026-07-08

Regulatory Status

RX

2026

30 Mar

RX Application: 220626

Drug Name

EPINEPHRINE

Product Number

1

Dosage Form

-

Strength

1MG/ML (1MG/ML)

Approval Date

2026-03-30

220626 / 1 View Details

Active Ingredient

EPINEPHRINE

Application Number

220626

Product Number

1

Dosage Form

-

Strength

1MG/ML (1MG/ML)

Approval Date

2026-03-30

Regulatory Status

RX

2026

30 Mar

RX Application: 220626

Drug Name

EPINEPHRINE

Product Number

2

Dosage Form

-

Strength

30MG/30ML (1MG/ML)

Approval Date

2026-03-30

220626 / 2 View Details

Active Ingredient

EPINEPHRINE

Application Number

220626

Product Number

2

Dosage Form

-

Strength

30MG/30ML (1MG/ML)

Approval Date

2026-03-30

Regulatory Status

RX

2026

16 Mar

RX Application: 218475

Drug Name

EPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2026-03-16

218475 / 2 View Details

Active Ingredient

EPINEPHRINE BITARTRATE

Application Number

218475

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2026-03-16

Regulatory Status

RX

2018

23 Nov

RX Application: 208554

Drug Name

EPTIFIBATIDE

Product Number

2

Dosage Form

-

Strength

75MG/100ML

Approval Date

2018-11-23

208554 / 2 View Details

Active Ingredient

EPTIFIBATIDE

Application Number

208554

Product Number

2

Dosage Form

-

Strength

75MG/100ML

Approval Date

2018-11-23

Regulatory Status

RX

2024

01 Oct

RX Application: 217250

Drug Name

ERIBULIN MESYLATE

Product Number

1

Dosage Form

-

Strength

1MG/2ML (0.5MG/ML)

Approval Date

2024-10-01

217250 / 1 View Details

Active Ingredient

ERIBULIN MESYLATE

Application Number

217250

Product Number

1

Dosage Form

-

Strength

1MG/2ML (0.5MG/ML)

Approval Date

2024-10-01

Regulatory Status

RX

2001

10 May

RX Application: 75591

Drug Name

FAMOTIDINE PRESERVATIVE FREE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2001-05-10

75591 / 1 View Details

Active Ingredient

FAMOTIDINE

Application Number

75591

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2001-05-10

Regulatory Status

RX

1982

01 Jan

RX Application: 18657

Drug Name

FLAGYL I.V. RTU IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1982-01-01

18657 / 1 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18657

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

2004

29 Jul

RX Application: 76766

Drug Name

FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

200MG/100ML (2MG/ML)

Approval Date

2004-07-29

76766 / 1 View Details

Active Ingredient

FLUCONAZOLE

Application Number

76766

Product Number

1

Dosage Form

-

Strength

200MG/100ML (2MG/ML)

Approval Date

2004-07-29

Regulatory Status

RX

2004

29 Jul

RX Application: 76766

Drug Name

FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

400MG/200ML (2MG/ML)

Approval Date

2004-07-29

76766 / 2 View Details

Active Ingredient

FLUCONAZOLE

Application Number

76766

Product Number

2

Dosage Form

-

Strength

400MG/200ML (2MG/ML)

Approval Date

2004-07-29

Regulatory Status

RX

2004

12 Oct

RX Application: 76755

Drug Name

FLUMAZENIL

Product Number

1

Dosage Form

-

Strength

1MG/10ML (0.1MG/ML)

Approval Date

2004-10-12

76755 / 1 View Details

Active Ingredient

FLUMAZENIL

Application Number

76755

Product Number

1

Dosage Form

-

Strength

1MG/10ML (0.1MG/ML)

Approval Date

2004-10-12

Regulatory Status

RX

2004

12 Oct

RX Application: 76755

Drug Name

FLUMAZENIL

Product Number

2

Dosage Form

-

Strength

0.5MG/5ML (0.1MG/ML)

Approval Date

2004-10-12

76755 / 2 View Details

Active Ingredient

FLUMAZENIL

Application Number

76755

Product Number

2

Dosage Form

-

Strength

0.5MG/5ML (0.1MG/ML)

Approval Date

2004-10-12

Regulatory Status

RX

1982

01 Jan

RX Application: 17624

Drug Name

FORANE

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

1982-01-01

17624 / 1 View Details

Active Ingredient

ISOFLURANE

Application Number

17624

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

1982-01-01

Regulatory Status

RX

2014

27 Jan

RX Application: 202747

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2014-01-27

202747 / 1 View Details

Active Ingredient

FUROSEMIDE

Application Number

202747

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2014-01-27

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1982-09-07

62373 / 2 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

2

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1982-09-07

62373 / 5 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

EQ 120MG BASE/100ML

Approval Date

1982-09-07

62373 / 6 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

6

Dosage Form

-

Strength

EQ 120MG BASE/100ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1982-09-07

62373 / 7 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

7

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1982-09-07

62373 / 8 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

8

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

07 Sep

RX Application: 62373

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1982-09-07

62373 / 9 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62373

Product Number

9

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1982-09-07

Regulatory Status

RX

1982

28 Apr

RX Application: 18609

Drug Name

HEPARIN SODIUM 1,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1982-04-28

18609 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

18609

Product Number

1

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1982

28 Apr

RX Application: 18609

Drug Name

HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1982-04-28

18609 / 2 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

18609

Product Number

2

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1982-04-28

Regulatory Status

RX

2025

17 Jul

RX Application: 219797

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2025-07-17

219797 / 1 View Details

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

219797

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2025-07-17

Regulatory Status

RX

1988

30 Dec

RX Application: 19763

Drug Name

IFEX

Product Number

1

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1988-12-30

19763 / 1 View Details

Active Ingredient

IFOSFAMIDE

Application Number

19763

Product Number

1

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1988-12-30

Regulatory Status

RX

1988

30 Dec

RX Application: 19763

Drug Name

IFEX

Product Number

2

Dosage Form

-

Strength

3GM/VIAL

Approval Date

1988-12-30

19763 / 2 View Details

Active Ingredient

IFOSFAMIDE

Application Number

19763

Product Number

2

Dosage Form

-

Strength

3GM/VIAL

Approval Date

1988-12-30

Regulatory Status

RX

2026

11 Aug

RX Application: 219684

Drug Name

KETAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE/5ML (EQ 10MG BASE/ML)

Approval Date

2026-08-11

219684 / 2 View Details

Active Ingredient

KETAMINE HYDROCHLORIDE

Application Number

219684

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE/5ML (EQ 10MG BASE/ML)

Approval Date

2026-08-11

Regulatory Status

RX

2017

15 Sep

RX Application: 209900

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2017-09-15

209900 / 1 View Details

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

209900

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2017-09-15

Regulatory Status

RX

2018

25 Jul

RX Application: 209900

Drug Name

KETOROLAC TROMETHAMINE

Product Number

2

Dosage Form

-

Strength

15MG/ML

Approval Date

2018-07-25

209900 / 2 View Details

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

209900

Product Number

2

Dosage Form

-

Strength

15MG/ML

Approval Date

2018-07-25

Regulatory Status

RX

2002

05 Jul

RX Application: 76051

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

2002-07-05

76051 / 1 View Details

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

76051

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

2002-07-05

Regulatory Status

RX

1982

01 Jan

RX Application: 16679

Drug Name

LACTATED RINGERS AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1982-01-01

16679 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

16679

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16682

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

16682 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

16682

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

RX

1982

19 Feb

RX Application: 18494

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-02-19

18494 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18494

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-02-19

Regulatory Status

RX

1984

03 Apr

RX Application: 18921

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1984-04-03

18921 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18921

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1984-04-03

Regulatory Status

RX

2026

06 Aug

RX Application: 208458

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

500MG/5ML (100MG/ML)

Approval Date

2026-08-06

208458 / 1 View Details

Active Ingredient

LEVETIRACETAM

Application Number

208458

Product Number

1

Dosage Form

-

Strength

500MG/5ML (100MG/ML)

Approval Date

2026-08-06

Regulatory Status

RX

2023

02 Oct

RX Application: 217059

Drug Name

LEVETIRACETAM IN SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG/100ML (5MG/ML)

Approval Date

2023-10-02

217059 / 1 View Details

Active Ingredient

LEVETIRACETAM

Application Number

217059

Product Number

1

Dosage Form

-

Strength

500MG/100ML (5MG/ML)

Approval Date

2023-10-02

Regulatory Status

RX

2023

02 Oct

RX Application: 217059

Drug Name

LEVETIRACETAM IN SODIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2023-10-02

217059 / 2 View Details

Active Ingredient

LEVETIRACETAM

Application Number

217059

Product Number

2

Dosage Form

-

Strength

1GM/100ML (10MG/ML)

Approval Date

2023-10-02

Regulatory Status

RX

2023

02 Oct

RX Application: 217059

Drug Name

LEVETIRACETAM IN SODIUM CHLORIDE

Product Number

3

Dosage Form

-

Strength

1.5GM/100ML (15MG/ML)

Approval Date

2023-10-02

217059 / 3 View Details

Active Ingredient

LEVETIRACETAM

Application Number

217059

Product Number

3

Dosage Form

-

Strength

1.5GM/100ML (15MG/ML)

Approval Date

2023-10-02

Regulatory Status

RX

2026

02 Jul

RX Application: 217896

Drug Name

LEVOCARNITINE

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2026-07-02

217896 / 1 View Details

Active Ingredient

LEVOCARNITINE

Application Number

217896

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2026-07-02

Regulatory Status

RX

1982

01 Jan

RX Application: 18461

Drug Name

LIDOCAINE HYDROCHLORIDE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1982-01-01

18461 / 2 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18461

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 18461

Drug Name

LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1982-01-01

18461 / 3 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18461

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

22 Feb

RX Application: 18461

Drug Name

LIDOCAINE HYDROCHLORIDE 0.8% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

800MG/100ML

Approval Date

1982-02-22

18461 / 4 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18461

Product Number

4

Dosage Form

-

Strength

800MG/100ML

Approval Date

1982-02-22

Regulatory Status

RX

2026

08 Jan

RX Application: 211966

Drug Name

MAGNESIUM SULFATE

Product Number

4

Dosage Form

-

Strength

3GM/100ML (30MG/ML)

Approval Date

2026-01-08

211966 / 4 View Details

Active Ingredient

MAGNESIUM SULFATE

Application Number

211966

Product Number

4

Dosage Form

-

Strength

3GM/100ML (30MG/ML)

Approval Date

2026-01-08

Regulatory Status

RX

2020

11 Aug

RX Application: 211965

Drug Name

MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

1GM/100ML

Approval Date

2020-08-11

211965 / 1 View Details

Active Ingredient

MAGNESIUM SULFATE

Application Number

211965

Product Number

1

Dosage Form

-

Strength

1GM/100ML

Approval Date

2020-08-11

Regulatory Status

RX

2020

01 Jun

RX Application: 211966

Drug Name

MAGNESIUM SULFATE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2GM/50ML (40MG/ML)

Approval Date

2020-06-01

211966 / 1 View Details

Active Ingredient

MAGNESIUM SULFATE

Application Number

211966

Product Number

1

Dosage Form

-

Strength

2GM/50ML (40MG/ML)

Approval Date

2020-06-01

Regulatory Status

RX

2020

01 Jun

RX Application: 211966

Drug Name

MAGNESIUM SULFATE IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

4GM/50ML (80MG/ML)

Approval Date

2020-06-01

211966 / 2 View Details

Active Ingredient

MAGNESIUM SULFATE

Application Number

211966

Product Number

2

Dosage Form

-

Strength

4GM/50ML (80MG/ML)

Approval Date

2020-06-01

Regulatory Status

RX

2020

01 Jun

RX Application: 211966

Drug Name

MAGNESIUM SULFATE IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

4GM/100ML (40MG/ML)

Approval Date

2020-06-01

211966 / 3 View Details

Active Ingredient

MAGNESIUM SULFATE

Application Number

211966

Product Number

3

Dosage Form

-

Strength

4GM/100ML (40MG/ML)

Approval Date

2020-06-01

Regulatory Status

RX

1988

30 Dec

RX Application: 19884

Drug Name

MESNEX

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1988-12-30

19884 / 1 View Details

Active Ingredient

MESNA

Application Number

19884

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1988-12-30

Regulatory Status

RX

2002

21 Mar

RX Application: 20855

Drug Name

MESNEX

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2002-03-21

20855 / 1 View Details

Active Ingredient

MESNA

Application Number

20855

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2002-03-21

Regulatory Status

RX

2013

29 Apr

RX Application: 78950

Drug Name

METOPROLOL TARTRATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2013-04-29

78950 / 1 View Details

Active Ingredient

METOPROLOL TARTRATE

Application Number

78950

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2013-04-29

Regulatory Status

RX

2023

29 Sep

RX Application: 216142

Drug Name

MICAFUNGIN IN SODIUM CHLORIDE 0.9%

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/50ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

216142 / 1 View Details

Active Ingredient

MICAFUNGIN SODIUM

Application Number

216142

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/50ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

Regulatory Status

RX

2023

29 Sep

RX Application: 216142

Drug Name

MICAFUNGIN IN SODIUM CHLORIDE 0.9%

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE/100ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

216142 / 2 View Details

Active Ingredient

MICAFUNGIN SODIUM

Application Number

216142

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE/100ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

Regulatory Status

RX

2023

29 Sep

RX Application: 216142

Drug Name

MICAFUNGIN IN SODIUM CHLORIDE 0.9%

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE/150ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

216142 / 3 View Details

Active Ingredient

MICAFUNGIN SODIUM

Application Number

216142

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE/150ML (EQ 1MG BASE/ML)

Approval Date

2023-09-29

Regulatory Status

RX

2002

28 May

RX Application: 75834

Drug Name

MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)

Approval Date

2002-05-28

75834 / 1 View Details

Active Ingredient

MILRINONE LACTATE

Application Number

75834

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)

Approval Date

2002-05-28

Regulatory Status

RX

2002

28 May

RX Application: 75834

Drug Name

MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML)

Approval Date

2002-05-28

75834 / 2 View Details

Active Ingredient

MILRINONE LACTATE

Application Number

75834

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML)

Approval Date

2002-05-28

Regulatory Status

RX

1989

31 Oct

RX Application: 50655

Drug Name

NALLPEN IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/100ML

Approval Date

1989-10-31

50655 / 2 View Details

Active Ingredient

NAFCILLIN SODIUM

Application Number

50655

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/100ML

Approval Date

1989-10-31

Regulatory Status

RX

2021

29 Jan

RX Application: 214785

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2021-01-29

214785 / 1 View Details

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

214785

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2021-01-29

Regulatory Status

RX

2025

03 Jun

RX Application: 214785

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

2025-06-03

214785 / 2 View Details

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

214785

Product Number

2

Dosage Form

-

Strength

1MG/ML

Approval Date

2025-06-03

Regulatory Status

RX

2022

07 Nov

RX Application: 214792

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2022-11-07

214792 / 1 View Details

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

214792

Product Number

1

Dosage Form

-

Strength

0.4MG/ML

Approval Date

2022-11-07

Regulatory Status

RX

2010

16 Nov

RX Application: 22325

Drug Name

NEXTERONE

Product Number

2

Dosage Form

-

Strength

150MG/100ML (1.5MG/ML)

Approval Date

2010-11-16

22325 / 2 View Details

Active Ingredient

AMIODARONE HYDROCHLORIDE

Application Number

22325

Product Number

2

Dosage Form

-

Strength

150MG/100ML (1.5MG/ML)

Approval Date

2010-11-16

Regulatory Status

RX

2010

16 Nov

RX Application: 22325

Drug Name

NEXTERONE

Product Number

3

Dosage Form

-

Strength

360MG/200ML (1.8MG/ML)

Approval Date

2010-11-16

22325 / 3 View Details

Active Ingredient

AMIODARONE HYDROCHLORIDE

Application Number

22325

Product Number

3

Dosage Form

-

Strength

360MG/200ML (1.8MG/ML)

Approval Date

2010-11-16

Regulatory Status

RX

1989

29 Dec

RX Application: 19970

Drug Name

NITROGLYCERIN IN DEXTROSE 5%

Product Number

1

Dosage Form

-

Strength

10MG/100ML

Approval Date

1989-12-29

19970 / 1 View Details

Active Ingredient

NITROGLYCERIN

Application Number

19970

Product Number

1

Dosage Form

-

Strength

10MG/100ML

Approval Date

1989-12-29

Regulatory Status

RX

1989

29 Dec

RX Application: 19970

Drug Name

NITROGLYCERIN IN DEXTROSE 5%

Product Number

2

Dosage Form

-

Strength

20MG/100ML

Approval Date

1989-12-29

19970 / 2 View Details

Active Ingredient

NITROGLYCERIN

Application Number

19970

Product Number

2

Dosage Form

-

Strength

20MG/100ML

Approval Date

1989-12-29

Regulatory Status

RX

1989

29 Dec

RX Application: 19970

Drug Name

NITROGLYCERIN IN DEXTROSE 5%

Product Number

3

Dosage Form

-

Strength

40MG/100ML

Approval Date

1989-12-29

19970 / 3 View Details

Active Ingredient

NITROGLYCERIN

Application Number

19970

Product Number

3

Dosage Form

-

Strength

40MG/100ML

Approval Date

1989-12-29

Regulatory Status

RX

2012

27 Mar

RX Application: 40859

Drug Name

NOREPINEPHRINE BITARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2012-03-27

40859 / 1 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

40859

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2012-03-27

Regulatory Status

RX

2026

06 Feb

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2026-02-06

214313 / 4 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

4

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2026-02-06

Regulatory Status

RX

2026

06 Feb

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE

Product Number

5

Dosage Form

-

Strength

EQ 8MG BASE/250ML (EQ 32MCG BASE/ML)

Approval Date

2026-02-06

214313 / 5 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

5

Dosage Form

-

Strength

EQ 8MG BASE/250ML (EQ 32MCG BASE/ML)

Approval Date

2026-02-06

Regulatory Status

RX

2026

06 Feb

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE

Product Number

6

Dosage Form

-

Strength

EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)

Approval Date

2026-02-06

214313 / 6 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

6

Dosage Form

-

Strength

EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)

Approval Date

2026-02-06

Regulatory Status

RX

2021

15 Jan

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2021-01-15

214313 / 1 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/250ML (EQ 16MCG BASE/ML)

Approval Date

2021-01-15

Regulatory Status

RX

2021

15 Jan

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE/250ML (EQ 32MCG BASE/ML)

Approval Date

2021-01-15

214313 / 2 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE/250ML (EQ 32MCG BASE/ML)

Approval Date

2021-01-15

Regulatory Status

RX

2023

21 Nov

RX Application: 214313

Drug Name

NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE

Product Number

3

Dosage Form

-

Strength

EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)

Approval Date

2023-11-21

214313 / 3 View Details

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

214313

Product Number

3

Dosage Form

-

Strength

EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)

Approval Date

2023-11-21

Regulatory Status

RX

2013

22 Feb

RX Application: 78287

Drug Name

ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2013-02-22

78287 / 1 View Details

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

78287

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2013-02-22

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 10% IN WATER

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

13684 / 2 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 10% IN WATER IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

13684 / 6 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

6

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 15% IN WATER

Product Number

4

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

13684 / 4 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

4

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 15% IN WATER IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

13684 / 8 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

8

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 20% IN WATER

Product Number

3

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

13684 / 3 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

3

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 20% IN WATER IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

13684 / 7 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

7

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 5% IN WATER

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

13684 / 1 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 13684

Drug Name

OSMITROL 5% IN WATER IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

13684 / 5 View Details

Active Ingredient

MANNITOL

Application Number

13684

Product Number

5

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

2024

14 Feb

RX Application: 217512

Drug Name

PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/100ML (EQ 0.4MG BASE/ML)

Approval Date

2024-02-14

217512 / 1 View Details

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

217512

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/100ML (EQ 0.4MG BASE/ML)

Approval Date

2024-02-14

Regulatory Status

RX

2024

14 Feb

RX Application: 217512

Drug Name

PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/50ML (EQ 0.8MG BASE/ML)

Approval Date

2024-02-14

217512 / 2 View Details

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

217512

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE/50ML (EQ 0.8MG BASE/ML)

Approval Date

2024-02-14

Regulatory Status

RX

2024

14 Feb

RX Application: 217512

Drug Name

PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 80MG BASE/100ML (EQ 0.8MG BASE/ML)

Approval Date

2024-02-14

217512 / 3 View Details

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

217512

Product Number

3

Dosage Form

-

Strength

EQ 80MG BASE/100ML (EQ 0.8MG BASE/ML)

Approval Date

2024-02-14

Regulatory Status

RX

1990

25 Jun

RX Application: 50638

Drug Name

PENICILLIN G POTASSIUM IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

1990-06-25

50638 / 1 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

50638

Product Number

1

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

1990-06-25

Regulatory Status

RX

1990

25 Jun

RX Application: 50638

Drug Name

PENICILLIN G POTASSIUM IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

40,000 UNITS/ML

Approval Date

1990-06-25

50638 / 2 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

50638

Product Number

2

Dosage Form

-

Strength

40,000 UNITS/ML

Approval Date

1990-06-25

Regulatory Status

RX

1990

25 Jun

RX Application: 50638

Drug Name

PENICILLIN G POTASSIUM IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

60,000 UNITS/ML

Approval Date

1990-06-25

50638 / 3 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

50638

Product Number

3

Dosage Form

-

Strength

60,000 UNITS/ML

Approval Date

1990-06-25

Regulatory Status

RX

2026

03 Apr

RX Application: 217032

Drug Name

PHENYLEPHRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML (10MG/ML)

Approval Date

2026-04-03

217032 / 1 View Details

Active Ingredient

PHENYLEPHRINE HYDROCHLORIDE

Application Number

217032

Product Number

1

Dosage Form

-

Strength

10MG/ML (10MG/ML)

Approval Date

2026-04-03

Regulatory Status

RX

2026

03 Apr

RX Application: 217032

Drug Name

PHENYLEPHRINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2026-04-03

217032 / 2 View Details

Active Ingredient

PHENYLEPHRINE HYDROCHLORIDE

Application Number

217032

Product Number

2

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2026-04-03

Regulatory Status

RX

2026

03 Apr

RX Application: 217032

Drug Name

PHENYLEPHRINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

2026-04-03

217032 / 3 View Details

Active Ingredient

PHENYLEPHRINE HYDROCHLORIDE

Application Number

217032

Product Number

3

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

2026-04-03

Regulatory Status

RX

2026

26 Feb

RX Application: 216852

Drug Name

PHYTONADIONE

Product Number

1

Dosage Form

-

Strength

1MG/0.5ML

Approval Date

2026-02-26

216852 / 1 View Details

Active Ingredient

PHYTONADIONE

Application Number

216852

Product Number

1

Dosage Form

-

Strength

1MG/0.5ML

Approval Date

2026-02-26

Regulatory Status

RX

1982

01 Jan

RX Application: 17378

Drug Name

PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Approval Date

1982-01-01

17378 / 1 View Details

Active Ingredient

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Application Number

17378

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

22 Nov

RX Application: 17378

Drug Name

PLASMA-LYTE A IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Approval Date

1982-11-22

17378 / 2 View Details

Active Ingredient

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Application Number

17378

Product Number

2

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Approval Date

1982-11-22

Regulatory Status

RX

2002

26 Nov

RX Application: 17648

Drug Name

POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%

Product Number

5

Dosage Form

-

Strength

150MG/100ML;450MG/100ML

Approval Date

2002-11-26

17648 / 5 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

17648

Product Number

5

Dosage Form

-

Strength

150MG/100ML;450MG/100ML

Approval Date

2002-11-26

Regulatory Status

RX

1982

01 Jan

RX Application: 17648

Drug Name

POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9%

Product Number

1

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1982-01-01

17648 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

17648

Product Number

1

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17648

Drug Name

POTASSIUM CHLORIDE 0.3% AND SODIUM CHLORIDE 0.9%

Product Number

2

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1982-01-01

17648 / 2 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

17648

Product Number

2

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 2 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

2

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 3 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

3

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1982

28 Apr

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;450MG/100ML

Approval Date

1982-04-28

18008 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

5

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;450MG/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1982

28 Apr

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-04-28

18008 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

6

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

4

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1989

26 Dec

RX Application: 19904

Drug Name

POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

14.9MG/ML

Approval Date

1989-12-26

19904 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

19904

Product Number

1

Dosage Form

-

Strength

14.9MG/ML

Approval Date

1989-12-26

Regulatory Status

RX

1990

17 Dec

RX Application: 19904

Drug Name

POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

746MG/100ML

Approval Date

1990-12-17

19904 / 5 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

19904

Product Number

5

Dosage Form

-

Strength

746MG/100ML

Approval Date

1990-12-17

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 6 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

6

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 4 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

4

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 5 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

5

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1982

28 Apr

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-04-28

18008 / 7 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

7

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

3

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

5

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1989

26 Dec

RX Application: 19904

Drug Name

POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

29.8MG/ML

Approval Date

1989-12-26

19904 / 2 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

19904

Product Number

2

Dosage Form

-

Strength

29.8MG/ML

Approval Date

1989-12-26

Regulatory Status

RX

1990

17 Dec

RX Application: 19904

Drug Name

POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

1.49GM/100ML

Approval Date

1990-12-17

19904 / 6 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

19904

Product Number

6

Dosage Form

-

Strength

1.49GM/100ML

Approval Date

1990-12-17

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 7 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

7

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1982

28 Apr

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;450MG/100ML

Approval Date

1982-04-28

18008 / 8 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

8

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;450MG/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

6

Dosage Form

-

Strength

5GM/100ML;224MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 8 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

8

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1982

28 Apr

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1982-04-28

18008 / 9 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

9

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1982-04-28

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 7 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

7

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1989

26 Dec

RX Application: 19904

Drug Name

POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

2.98GM/100ML

Approval Date

1989-12-26

19904 / 4 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

19904

Product Number

4

Dosage Form

-

Strength

2.98GM/100ML

Approval Date

1989-12-26

Regulatory Status

RX

1985

05 Apr

RX Application: 19367

Drug Name

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

19367 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19367

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

1982

01 Jan

RX Application: 18008

Drug Name

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-01-01

18008 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18008

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1985

05 Apr

RX Application: 19308

Drug Name

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

19308 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19308

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1985-04-05

Regulatory Status

RX

2003

19 Jun

RX Application: 75880

Drug Name

PREMASOL 10% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

2003-06-19

75880 / 2 View Details

Active Ingredient

AMINO ACIDS

Application Number

75880

Product Number

2

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

2003-06-19

Regulatory Status

RX

2003

19 Jun

RX Application: 75880

Drug Name

PREMASOL 6% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

6% (6GM/100ML)

Approval Date

2003-06-19

75880 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

75880

Product Number

1

Dosage Form

-

Strength

6% (6GM/100ML)

Approval Date

2003-06-19

Regulatory Status

RX

1998

26 Aug

RX Application: 20849

Drug Name

PROSOL 20% SULFITE FREE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20% (20GM/100ML)

Approval Date

1998-08-26

20849 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

20849

Product Number

1

Dosage Form

-

Strength

20% (20GM/100ML)

Approval Date

1998-08-26

Regulatory Status

RX

1982

01 Jan

RX Application: 14134

Drug Name

PROTOPAM CHLORIDE

Product Number

1

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1982-01-01

14134 / 1 View Details

Active Ingredient

PRALIDOXIME CHLORIDE

Application Number

14134

Product Number

1

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1982-01-01

Regulatory Status

RX

2023

23 May

RX Application: 217455

Drug Name

REGADENOSON

Product Number

1

Dosage Form

-

Strength

0.4MG/5ML (0.08MG/ML)

Approval Date

2023-05-23

217455 / 1 View Details

Active Ingredient

REGADENOSON

Application Number

217455

Product Number

1

Dosage Form

-

Strength

0.4MG/5ML (0.08MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

1982

01 Jan

RX Application: 16693

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

16693 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

16693

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

RX

1982

19 Feb

RX Application: 18495

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-02-19

18495 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18495

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-02-19

Regulatory Status

RX

2002

02 Jul

RX Application: 75895

Drug Name

SEVOFLURANE

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

2002-07-02

75895 / 1 View Details

Active Ingredient

SEVOFLURANE

Application Number

75895

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

2002-07-02

Regulatory Status

RX

1982

01 Jan

RX Application: 18016

Drug Name

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1982-01-01

18016 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

18016

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16677

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

16677 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

16677

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16677

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

1982-01-01

16677 / 3 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

16677

Product Number

3

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

1982-01-01

Regulatory Status

RX

1985

30 Oct

RX Application: 16677

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

225MG/25ML (9MG/ML)

Approval Date

1985-10-30

16677 / 4 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

16677

Product Number

4

Dosage Form

-

Strength

225MG/25ML (9MG/ML)

Approval Date

1985-10-30

Regulatory Status

RX

1982

01 Jan

RX Application: 17427

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

17427 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

17427

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17867

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

17867 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

17867

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1992

07 Dec

RX Application: 20178

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1992-12-07

20178 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

20178

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1992-12-07

Regulatory Status

RX

1992

07 Dec

RX Application: 20178

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

1992-12-07

20178 / 2 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

20178

Product Number

2

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

1992-12-07

Regulatory Status

RX

1985

17 May

RX Application: 19319

Drug Name

SODIUM CHLORIDE 0.9% IN STERILE PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

1985-05-17

19319 / 2 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19319

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

1985-05-17

Regulatory Status

RX

1983

01 Nov

RX Application: 19022

Drug Name

SODIUM CHLORIDE 3% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3GM/100ML

Approval Date

1983-11-01

19022 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19022

Product Number

1

Dosage Form

-

Strength

3GM/100ML

Approval Date

1983-11-01

Regulatory Status

RX

1983

01 Nov

RX Application: 19022

Drug Name

SODIUM CHLORIDE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1983-11-01

19022 / 2 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19022

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1983-11-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17863

Drug Name

SORBITOL 3% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3GM/100ML

Approval Date

1982-01-01

17863 / 1 View Details

Active Ingredient

SORBITOL

Application Number

17863

Product Number

1

Dosage Form

-

Strength

3GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17428

Drug Name

STERILE WATER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

17428 / 1 View Details

Active Ingredient

STERILE WATER FOR IRRIGATION

Application Number

17428

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

Regulatory Status

RX

1982

30 Jun

RX Application: 18632

Drug Name

STERILE WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-06-30

18632 / 1 View Details

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

18632

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-06-30

Regulatory Status

RX

1988

19 Apr

RX Application: 18632

Drug Name

STERILE WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

100%

Approval Date

1988-04-19

18632 / 2 View Details

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

18632

Product Number

2

Dosage Form

-

Strength

100%

Approval Date

1988-04-19

Regulatory Status

RX

1982

01 Jan

RX Application: 17866

Drug Name

STERILE WATER IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

17866 / 1 View Details

Active Ingredient

STERILE WATER FOR IRRIGATION

Application Number

17866

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

Regulatory Status

RX

2024

24 Sep

RX Application: 218878

Drug Name

SUCCINYLCHOLINE CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2024-09-24

218878 / 1 View Details

Active Ingredient

SUCCINYLCHOLINE CHLORIDE

Application Number

218878

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2024-09-24

Regulatory Status

RX

1992

18 Sep

RX Application: 20118

Drug Name

SUPRANE

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1992-09-18

20118 / 1 View Details

Active Ingredient

DESFLURANE

Application Number

20118

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1992-09-18

Regulatory Status

RX

1982

19 Feb

RX Application: 18508

Drug Name

TIS-U-SOL

Product Number

1

Dosage Form

-

Strength

20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Approval Date

1982-02-19

18508 / 1 View Details

Active Ingredient

MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

Application Number

18508

Product Number

1

Dosage Form

-

Strength

20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Approval Date

1982-02-19

Regulatory Status

RX

1982

01 Jan

RX Application: 18336

Drug Name

TIS-U-SOL IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Approval Date

1982-01-01

18336 / 1 View Details

Active Ingredient

MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

Application Number

18336

Product Number

1

Dosage Form

-

Strength

20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

2016

01 Jul

RX Application: 206965

Drug Name

TOBRAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

2016-07-01

206965 / 1 View Details

Active Ingredient

TOBRAMYCIN SULFATE

Application Number

206965

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

2016-07-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17874

Drug Name

TRANSDERM SCOP

Product Number

1

Dosage Form

-

Strength

1MG/72HR

Approval Date

1982-01-01

17874 / 1 View Details

Active Ingredient

SCOPOLAMINE

Application Number

17874

Product Number

1

Dosage Form

-

Strength

1MG/72HR

Approval Date

1982-01-01

Regulatory Status

RX

1984

23 Aug

RX Application: 18931

Drug Name

TRAVASOL 10% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

10% (10MG/100ML)

Approval Date

1984-08-23

18931 / 3 View Details

Active Ingredient

AMINO ACIDS

Application Number

18931

Product Number

3

Dosage Form

-

Strength

10% (10MG/100ML)

Approval Date

1984-08-23

Regulatory Status

RX

1984

23 Aug

RX Application: 18931

Drug Name

TRAVASOL 5.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5.5% (5.5GM/100ML)

Approval Date

1984-08-23

18931 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

18931

Product Number

1

Dosage Form

-

Strength

5.5% (5.5GM/100ML)

Approval Date

1984-08-23

Regulatory Status

RX

1984

23 Aug

RX Application: 18931

Drug Name

TRAVASOL 8.5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1984-08-23

18931 / 2 View Details

Active Ingredient

AMINO ACIDS

Application Number

18931

Product Number

2

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1984-08-23

Regulatory Status

RX

1993

29 Apr

RX Application: 50671

Drug Name

VANCOMYCIN HYDROCHLORIDE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/100ML (EQ 5MG BASE/ML)

Approval Date

1993-04-29

50671 / 1 View Details

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

50671

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/100ML (EQ 5MG BASE/ML)

Approval Date

1993-04-29

Regulatory Status

RX

2010

20 Dec

RX Application: 50671

Drug Name

VANCOMYCIN HYDROCHLORIDE IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE/150ML (EQ 5MG BASE/ML)

Approval Date

2010-12-20

50671 / 2 View Details

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

50671

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE/150ML (EQ 5MG BASE/ML)

Approval Date

2010-12-20

Regulatory Status

RX

1999

01 Mar

RX Application: 50671

Drug Name

VANCOMYCIN HYDROCHLORIDE IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/200ML (EQ 5MG BASE/ML)

Approval Date

1999-03-01

50671 / 3 View Details

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

50671

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/200ML (EQ 5MG BASE/ML)

Approval Date

1999-03-01

Regulatory Status

RX

2024

25 Jan

RX Application: 50671

Drug Name

VANCOMYCIN HYDROCHLORIDE IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

EQ 1.25GM BASE/250ML (EQ 5MG BASE/ML)

Approval Date

2024-01-25

50671 / 4 View Details

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

50671

Product Number

4

Dosage Form

-

Strength

EQ 1.25GM BASE/250ML (EQ 5MG BASE/ML)

Approval Date

2024-01-25

Regulatory Status

RX

2024

25 Jan

RX Application: 50671

Drug Name

VANCOMYCIN HYDROCHLORIDE IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

EQ 1.5GM BASE/300ML (EQ 5MG BASE/ML)

Approval Date

2024-01-25

50671 / 5 View Details

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

50671

Product Number

5

Dosage Form

-

Strength

EQ 1.5GM BASE/300ML (EQ 5MG BASE/ML)

Approval Date

2024-01-25

Regulatory Status

RX

2023

29 Sep

RX Application: 217569

Drug Name

VASOPRESSIN IN SODIUM CHLORIDE 0.9%

Product Number

1

Dosage Form

-

Strength

20UNITS/100ML (0.2UNITS/ML)

Approval Date

2023-09-29

217569 / 1 View Details

Active Ingredient

VASOPRESSIN

Application Number

217569

Product Number

1

Dosage Form

-

Strength

20UNITS/100ML (0.2UNITS/ML)

Approval Date

2023-09-29

Regulatory Status

RX

2023

29 Sep

RX Application: 217569

Drug Name

VASOPRESSIN IN SODIUM CHLORIDE 0.9%

Product Number

2

Dosage Form

-

Strength

40UNITS/100ML (0.4UNITS/ML)

Approval Date

2023-09-29

217569 / 2 View Details

Active Ingredient

VASOPRESSIN

Application Number

217569

Product Number

2

Dosage Form

-

Strength

40UNITS/100ML (0.4UNITS/ML)

Approval Date

2023-09-29

Regulatory Status

RX

1998

24 Feb

RX Application: 50750

Drug Name

ZOSYN IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML;EQ 5MG BASE/ML

Approval Date

1998-02-24

50750 / 1 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

50750

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML;EQ 5MG BASE/ML

Approval Date

1998-02-24

Regulatory Status

RX

1998

24 Feb

RX Application: 50750

Drug Name

ZOSYN IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 60MG BASE/ML;EQ 7.5MG BASE/ML

Approval Date

1998-02-24

50750 / 2 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

50750

Product Number

2

Dosage Form

-

Strength

EQ 60MG BASE/ML;EQ 7.5MG BASE/ML

Approval Date

1998-02-24

Regulatory Status

RX

1998

24 Feb

RX Application: 50750

Drug Name

ZOSYN IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/100ML;EQ 500MG BASE/100ML

Approval Date

1998-02-24

50750 / 3 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

50750

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/100ML;EQ 500MG BASE/100ML

Approval Date

1998-02-24

Regulatory Status

RX

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