B. Braun Medical

1982

29 Nov

Discontinued Application: 18725

Drug Name

ACETATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;30MG/100ML;380MG/100ML;600MG/100ML

Approval Date

1982-11-29

18725 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18725

Product Number

1

Dosage Form

-

Strength

20MG/100ML;30MG/100ML;380MG/100ML;600MG/100ML

Approval Date

1982-11-29

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 18161

Drug Name

ACETIC ACID 0.25% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

250MG/100ML

Approval Date

1982-01-01

18161 / 1 View Details

Active Ingredient

ACETIC ACID, GLACIAL

Application Number

18161

Product Number

1

Dosage Form

-

Strength

250MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

-

Unclassified Application: 4589

Drug Name

ALCOHOL 5% AND DEXTROSE 5%

Product Number

4

Dosage Form

-

Strength

5ML/100ML;5GM/100ML

Approval Date

-

4589 / 4 View Details

Active Ingredient

ALCOHOL; DEXTROSE

Application Number

4589

Product Number

4

Dosage Form

-

Strength

5ML/100ML;5GM/100ML

Approval Date

-

Regulatory Status

Unclassified

2012

13 Apr

RX Application: 91112

Drug Name

AMINO ACIDS

Product Number

1

Dosage Form

-

Strength

15%(150GM/1000ML)

Approval Date

2012-04-13

91112 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

91112

Product Number

1

Dosage Form

-

Strength

15%(150GM/1000ML)

Approval Date

2012-04-13

Regulatory Status

RX

2012

13 Apr

RX Application: 91112

Drug Name

AMINO ACIDS

Product Number

2

Dosage Form

-

Strength

15%(300GM/2000ML)

Approval Date

2012-04-13

91112 / 2 View Details

Active Ingredient

AMINO ACIDS

Application Number

91112

Product Number

2

Dosage Form

-

Strength

15%(300GM/2000ML)

Approval Date

2012-04-13

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 85734

Drug Name

AMMONIUM CHLORIDE 2.14%

Product Number

1

Dosage Form

-

Strength

40MEQ/100ML

Approval Date

1982-01-01

85734 / 1 View Details

Active Ingredient

AMMONIUM CHLORIDE

Application Number

85734

Product Number

1

Dosage Form

-

Strength

40MEQ/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2010

03 Feb

RX Application: 91387

Drug Name

BALANCED SALT

Product Number

1

Dosage Form

-

Strength

0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML

Approval Date

2010-02-03

91387 / 1 View Details

Active Ingredient

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

Application Number

91387

Product Number

1

Dosage Form

-

Strength

0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML

Approval Date

2010-02-03

Regulatory Status

RX

1986

29 Apr

Discontinued Application: 19121

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100MG/100ML

Approval Date

1986-04-29

19121 / 1 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19121

Product Number

1

Dosage Form

-

Strength

100MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1986

29 Apr

Discontinued Application: 19121

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1986-04-29

19121 / 2 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19121

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

1986

29 Apr

Discontinued Application: 19121

Drug Name

BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1986-04-29

19121 / 3 View Details

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

19121

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1986-04-29

Regulatory Status

Discontinued

2000

27 Jul

Discontinued Application: 50779

Drug Name

CEFAZOLIN AND DEXTROSE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2000-07-27

50779 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

50779

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2000-07-27

Regulatory Status

Discontinued

2000

27 Jul

RX Application: 50779

Drug Name

CEFAZOLIN AND DEXTROSE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2000-07-27

50779 / 2 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

50779

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2000-07-27

Regulatory Status

RX

2012

13 Jan

RX Application: 50779

Drug Name

CEFAZOLIN AND DEXTROSE

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2012-01-13

50779 / 3 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

50779

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2012-01-13

Regulatory Status

RX

2024

26 Aug

RX Application: 50779

Drug Name

CEFAZOLIN AND DEXTROSE

Product Number

4

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2024-08-26

50779 / 4 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

50779

Product Number

4

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2024-08-26

Regulatory Status

RX

2010

06 May

RX Application: 50821

Drug Name

CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2010-05-06

50821 / 1 View Details

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

50821

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2010-05-06

Regulatory Status

RX

2010

06 May

RX Application: 50821

Drug Name

CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2010-05-06

50821 / 2 View Details

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

50821

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2010-05-06

Regulatory Status

RX

2004

29 Jul

Discontinued Application: 50792

Drug Name

CEFOTAXIME AND DEXTROSE 2.4% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE

Approval Date

2004-07-29

50792 / 1 View Details

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50792

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004

29 Jul

Discontinued Application: 50792

Drug Name

CEFOTAXIME AND DEXTROSE 3.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2004-07-29

50792 / 2 View Details

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50792

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2004-07-29

Regulatory Status

Discontinued

2007

09 Aug

Discontinued Application: 65430

Drug Name

CEFOTETAN AND DEXTROSE IN DUPLEX CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2007-08-09

65430 / 1 View Details

Active Ingredient

CEFOTETAN DISODIUM

Application Number

65430

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2007-08-09

Regulatory Status

Discontinued

2007

09 Aug

Discontinued Application: 65430

Drug Name

CEFOTETAN AND DEXTROSE IN DUPLEX CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2007-08-09

65430 / 2 View Details

Active Ingredient

CEFOTETAN DISODIUM

Application Number

65430

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2007-08-09

Regulatory Status

Discontinued

2006

10 Mar

RX Application: 65214

Drug Name

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2006-03-10

65214 / 1 View Details

Active Ingredient

CEFOXITIN SODIUM

Application Number

65214

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2006-03-10

Regulatory Status

RX

2006

10 Mar

RX Application: 65214

Drug Name

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2006-03-10

65214 / 2 View Details

Active Ingredient

CEFOXITIN SODIUM

Application Number

65214

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2006-03-10

Regulatory Status

RX

2011

13 Jun

Discontinued Application: 50823

Drug Name

CEFTAZIDIME IN DEXTROSE CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2011-06-13

50823 / 1 View Details

Active Ingredient

CEFTAZIDIME

Application Number

50823

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2011-06-13

Regulatory Status

Discontinued

2011

13 Jun

Discontinued Application: 50823

Drug Name

CEFTAZIDIME IN DEXTROSE CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE

Approval Date

2011-06-13

50823 / 2 View Details

Active Ingredient

CEFTAZIDIME

Application Number

50823

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE

Approval Date

2011-06-13

Regulatory Status

Discontinued

2005

20 Apr

RX Application: 50796

Drug Name

CEFTRIAXONE AND DEXTROSE IN DUPLEX CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2005-04-20

50796 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

50796

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2005-04-20

Regulatory Status

RX

2005

20 Apr

RX Application: 50796

Drug Name

CEFTRIAXONE AND DEXTROSE IN DUPLEX CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2005-04-20

50796 / 2 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

50796

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2005-04-20

Regulatory Status

RX

2001

21 Feb

Discontinued Application: 50780

Drug Name

CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

2001-02-21

50780 / 1 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

50780

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

2001-02-21

Regulatory Status

Discontinued

2001

21 Feb

Discontinued Application: 50780

Drug Name

CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

2001-02-21

50780 / 2 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

50780

Product Number

2

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

2001-02-21

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

10GM/100ML;110MG/100ML

Approval Date

1988-02-24

19631 / 11 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

11

Dosage Form

-

Strength

10GM/100ML;110MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18386

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10GM/100ML;200MG/100ML

Approval Date

1982-01-01

18386 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18386

Product Number

1

Dosage Form

-

Strength

10GM/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

12

Dosage Form

-

Strength

10GM/100ML;200MG/100ML

Approval Date

1988-02-24

19631 / 12 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

12

Dosage Form

-

Strength

10GM/100ML;200MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

13

Dosage Form

-

Strength

10GM/100ML;330MG/100ML

Approval Date

1988-02-24

19631 / 13 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

13

Dosage Form

-

Strength

10GM/100ML;330MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18229

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10GM/100ML;450MG/100ML

Approval Date

1982-01-01

18229 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18229

Product Number

1

Dosage Form

-

Strength

10GM/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

14

Dosage Form

-

Strength

10GM/100ML;450MG/100ML

Approval Date

1988-02-24

19631 / 14 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

14

Dosage Form

-

Strength

10GM/100ML;450MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18047

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10GM/100ML;900MG/100ML

Approval Date

1982-01-01

18047 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18047

Product Number

1

Dosage Form

-

Strength

10GM/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

15

Dosage Form

-

Strength

10GM/100ML;900MG/100ML

Approval Date

1988-02-24

19631 / 15 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

15

Dosage Form

-

Strength

10GM/100ML;900MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18046

Drug Name

DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

18046 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

18046

Product Number

1

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

02 Feb

RX Application: 19626

Drug Name

DEXTROSE 10% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

10GM/100ML

Approval Date

1988-02-02

19626 / 4 View Details

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

4

Dosage Form

-

Strength

10GM/100ML

Approval Date

1988-02-02

Regulatory Status

RX

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;110MG/100ML

Approval Date

1988-02-24

19631 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;110MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

2.5GM/100ML;200MG/100ML

Approval Date

1988-02-24

19631 / 2 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

2

Dosage Form

-

Strength

2.5GM/100ML;200MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

2.5GM/100ML;330MG/100ML

Approval Date

1988-02-24

19631 / 3 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

3

Dosage Form

-

Strength

2.5GM/100ML;330MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18030

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

18030 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18030

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

2.5GM/100ML;450MG/100ML

Approval Date

1988-02-24

19631 / 4 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

4

Dosage Form

-

Strength

2.5GM/100ML;450MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18376

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;900MG/100ML

Approval Date

1982-01-01

18376 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18376

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

2.5GM/100ML;900MG/100ML

Approval Date

1988-02-24

19631 / 5 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

5

Dosage Form

-

Strength

2.5GM/100ML;900MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1988

24 Feb

RX Application: 19634

Drug Name

DEXTROSE 2.5% IN HALF-STRENGTH LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

10MG/100ML;2.5GM/100ML;15MG/100ML;300MG/100ML;160MG/100ML

Approval Date

1988-02-24

19634 / 1 View Details

Active Ingredient

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

Application Number

19634

Product Number

1

Dosage Form

-

Strength

10MG/100ML;2.5GM/100ML;15MG/100ML;300MG/100ML;160MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18358

Drug Name

DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML

Approval Date

1982-01-01

18358 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

18358

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

02 Feb

Discontinued Application: 19626

Drug Name

DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML

Approval Date

1988-02-02

19626 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

1

Dosage Form

-

Strength

2.5GM/100ML

Approval Date

1988-02-02

Regulatory Status

Discontinued

1990

19 Jan

RX Application: 19631

Drug Name

DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

16

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML

Approval Date

1990-01-19

19631 / 16 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

16

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML

Approval Date

1990-01-19

Regulatory Status

RX

1988

24 Feb

Discontinued Application: 19634

Drug Name

DEXTROSE 4% IN MODIFIED LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

4MG/100ML;4GM/100ML;6MG/100ML;120MG/100ML;62MG/100ML

Approval Date

1988-02-24

19634 / 2 View Details

Active Ingredient

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

Application Number

19634

Product Number

2

Dosage Form

-

Strength

4MG/100ML;4GM/100ML;6MG/100ML;120MG/100ML;62MG/100ML

Approval Date

1988-02-24

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18030

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1982-01-01

18030 / 5 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18030

Product Number

5

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1988-02-24

19631 / 6 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

6

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18030

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1982-01-01

18030 / 4 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18030

Product Number

4

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1988-02-24

19631 / 7 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

7

Dosage Form

-

Strength

5GM/100ML;200MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18030

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1982-01-01

18030 / 3 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18030

Product Number

3

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1988-02-24

19631 / 8 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

8

Dosage Form

-

Strength

5GM/100ML;330MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18030

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1982-01-01

18030 / 2 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18030

Product Number

2

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1988-02-24

19631 / 9 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

9

Dosage Form

-

Strength

5GM/100ML;450MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18026

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1982-01-01

18026 / 1 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

18026

Product Number

1

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19631

Drug Name

DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

10

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1988-02-24

19631 / 10 View Details

Active Ingredient

DEXTROSE; SODIUM CHLORIDE

Application Number

19631

Product Number

10

Dosage Form

-

Strength

5GM/100ML;900MG/100ML

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18258

Drug Name

DEXTROSE 5% IN ACETATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;30MG/100ML;380MG/100ML;600MG/100ML

Approval Date

1982-01-01

18258 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18258

Product Number

1

Dosage Form

-

Strength

20MG/100ML;5GM/100ML;30MG/100ML;380MG/100ML;600MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17510

Drug Name

DEXTROSE 5% IN LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17510 / 1 View Details

Active Ingredient

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

Application Number

17510

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

24 Feb

RX Application: 19634

Drug Name

DEXTROSE 5% IN LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1988-02-24

19634 / 3 View Details

Active Ingredient

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

Application Number

19634

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1988-02-24

Regulatory Status

RX

1982

01 Jan

RX Application: 16730

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16730 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

16730

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 16730

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

16730 / 2 View Details

Active Ingredient

DEXTROSE

Application Number

16730

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

RX

1988

02 Feb

RX Application: 19626

Drug Name

DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1988-02-02

19626 / 2 View Details

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1988-02-02

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18256

Drug Name

DEXTROSE 5% IN RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML

Approval Date

1982-01-01

18256 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18256

Product Number

1

Dosage Form

-

Strength

33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992

17 Apr

Discontinued Application: 20000

Drug Name

DEXTROSE 5% IN RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML

Approval Date

1992-04-17

20000 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

20000

Product Number

1

Dosage Form

-

Strength

33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML

Approval Date

1992-04-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.075%

Product Number

9

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 9 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

9

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.224% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1982-01-01

18268 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

6

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

18 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

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

Approval Date

1986-01-18

18268 / 11 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

11

Dosage Form

-

Strength

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

Approval Date

1986-01-18

Regulatory Status

Discontinued

1986

18 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER

Product Number

12

Dosage Form

-

Strength

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

Approval Date

1986-01-18

18268 / 12 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

12

Dosage Form

-

Strength

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

Approval Date

1986-01-18

Regulatory Status

Discontinued

1986

18 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER

Product Number

13

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;330MG/100ML

Approval Date

1986-01-18

18268 / 13 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

13

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;330MG/100ML

Approval Date

1986-01-18

Regulatory Status

Discontinued

1986

18 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.30% IN PLASTIC CONTAINER

Product Number

14

Dosage Form

-

Strength

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

Approval Date

1986-01-18

18268 / 14 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

14

Dosage Form

-

Strength

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

Approval Date

1986-01-18

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.075%

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 10 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1982-01-01

18268 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

2

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18268

Drug Name

DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18268 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18268

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

22 Sep

Discontinued Application: 17995

Drug Name

DEXTROSE 60%

Product Number

2

Dosage Form

-

Strength

60GM/100ML

Approval Date

1982-09-22

17995 / 2 View Details

Active Ingredient

DEXTROSE

Application Number

17995

Product Number

2

Dosage Form

-

Strength

60GM/100ML

Approval Date

1982-09-22

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17995

Drug Name

DEXTROSE 60% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

60GM/100ML

Approval Date

1982-01-01

17995 / 1 View Details

Active Ingredient

DEXTROSE

Application Number

17995

Product Number

1

Dosage Form

-

Strength

60GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

02 Feb

Discontinued Application: 19626

Drug Name

DEXTROSE 7.7% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

7.7GM/100ML

Approval Date

1988-02-02

19626 / 3 View Details

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

3

Dosage Form

-

Strength

7.7GM/100ML

Approval Date

1988-02-02

Regulatory Status

Discontinued

2015

18 Feb

RX Application: 19626

Drug Name

DEXTROSE 70% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

70GM/100ML

Approval Date

2015-02-18

19626 / 5 View Details

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

5

Dosage Form

-

Strength

70GM/100ML

Approval Date

2015-02-18

Regulatory Status

RX

1983

26 Aug

Discontinued Application: 18807

Drug Name

DIALYTE CONCENTRATE W/ DEXTROSE 30% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

510MG/100ML;30GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML

Approval Date

1983-08-26

18807 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18807

Product Number

1

Dosage Form

-

Strength

510MG/100ML;30GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML

Approval Date

1983-08-26

Regulatory Status

Discontinued

1983

26 Aug

Discontinued Application: 18807

Drug Name

DIALYTE CONCENTRATE W/ DEXTROSE 30% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

510MG/100ML;30GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML

Approval Date

1983-08-26

18807 / 3 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18807

Product Number

3

Dosage Form

-

Strength

510MG/100ML;30GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML

Approval Date

1983-08-26

Regulatory Status

Discontinued

1983

26 Aug

Discontinued Application: 18807

Drug Name

DIALYTE CONCENTRATE W/ DEXTROSE 50% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

510MG/100ML;50GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML

Approval Date

1983-08-26

18807 / 2 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18807

Product Number

2

Dosage Form

-

Strength

510MG/100ML;50GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML

Approval Date

1983-08-26

Regulatory Status

Discontinued

1983

26 Aug

Discontinued Application: 18807

Drug Name

DIALYTE CONCENTRATE W/ DEXTROSE 50% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

510MG/100ML;50GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML

Approval Date

1983-08-26

18807 / 4 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18807

Product Number

4

Dosage Form

-

Strength

510MG/100ML;50GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML

Approval Date

1983-08-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

26MG/100ML;1.5GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML

Approval Date

1982-01-01

18460 / 2 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

2

Dosage Form

-

Strength

26MG/100ML;1.5GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

29 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

26MG/100ML;1.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

18460 / 7 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

7

Dosage Form

-

Strength

26MG/100ML;1.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

Regulatory Status

Discontinued

1983

02 Nov

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

26MG/100ML;2.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1983-11-02

18460 / 5 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

5

Dosage Form

-

Strength

26MG/100ML;2.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1983-11-02

Regulatory Status

Discontinued

1986

29 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

29MG/100ML;2.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1986-01-29

18460 / 6 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18460

Product Number

6

Dosage Form

-

Strength

29MG/100ML;2.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1986-01-29

Regulatory Status

Discontinued

1986

29 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

26MG/100ML;5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

18460 / 8 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

8

Dosage Form

-

Strength

26MG/100ML;5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

26MG/100ML;4.25GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML

Approval Date

1982-01-01

18460 / 4 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

4

Dosage Form

-

Strength

26MG/100ML;4.25GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

29 Jan

Discontinued Application: 18460

Drug Name

DIALYTE LM/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

26MG/100ML;4.25GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

18460 / 9 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18460

Product Number

9

Dosage Form

-

Strength

26MG/100ML;4.25GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML

Approval Date

1986-01-29

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18460

Drug Name

DIALYTE W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

29MG/100ML;1.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1982-01-01

18460 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18460

Product Number

1

Dosage Form

-

Strength

29MG/100ML;1.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18460

Drug Name

DIALYTE W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

29MG/100ML;4.25GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1982-01-01

18460 / 3 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18460

Product Number

3

Dosage Form

-

Strength

29MG/100ML;4.25GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

15 Oct

Discontinued Application: 19099

Drug Name

DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1986-10-15

19099 / 2 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19099

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1986-10-15

Regulatory Status

Discontinued

1986

15 Oct

Discontinued Application: 19099

Drug Name

DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%

Product Number

4

Dosage Form

-

Strength

320MG/100ML

Approval Date

1986-10-15

19099 / 4 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19099

Product Number

4

Dosage Form

-

Strength

320MG/100ML

Approval Date

1986-10-15

Regulatory Status

Discontinued

1986

15 Oct

Discontinued Application: 19099

Drug Name

DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1986-10-15

19099 / 1 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19099

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1986-10-15

Regulatory Status

Discontinued

1986

15 Oct

Discontinued Application: 19099

Drug Name

DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1986-10-15

19099 / 3 View Details

Active Ingredient

DOPAMINE HYDROCHLORIDE

Application Number

19099

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1986-10-15

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16822

Drug Name

FREAMINE 8.5%

Product Number

1

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

16822 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

16822

Product Number

1

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983

17 May

Discontinued Application: 16822

Drug Name

FREAMINE HBC 6.9%

Product Number

6

Dosage Form

-

Strength

6.9% (6.9GM/100ML)

Approval Date

1983-05-17

16822 / 6 View Details

Active Ingredient

AMINO ACIDS

Application Number

16822

Product Number

6

Dosage Form

-

Strength

6.9% (6.9GM/100ML)

Approval Date

1983-05-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16822

Drug Name

FREAMINE II 8.5%

Product Number

2

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

16822 / 2 View Details

Active Ingredient

AMINO ACIDS

Application Number

16822

Product Number

2

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16822

Drug Name

FREAMINE III 10%

Product Number

5

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1982-01-01

16822 / 5 View Details

Active Ingredient

AMINO ACIDS

Application Number

16822

Product Number

5

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16822

Drug Name

FREAMINE III 3% W/ ELECTROLYTES

Product Number

3

Dosage Form

-

Strength

3%;54MG/100ML;40MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML

Approval Date

1982-01-01

16822 / 3 View Details

Active Ingredient

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

Application Number

16822

Product Number

3

Dosage Form

-

Strength

3%;54MG/100ML;40MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16822

Drug Name

FREAMINE III 8.5%

Product Number

4

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

16822 / 4 View Details

Active Ingredient

AMINO ACIDS

Application Number

16822

Product Number

4

Dosage Form

-

Strength

8.5% (8.5GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

01 Jul

Discontinued Application: 16822

Drug Name

FREAMINE III 8.5% W/ ELECTROLYTES

Product Number

7

Dosage Form

-

Strength

8.5%;110MG/100ML;230MG/100ML;10MG/100ML;440MG/100ML;690MG/100ML

Approval Date

1988-07-01

16822 / 7 View Details

Active Ingredient

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

Application Number

16822

Product Number

7

Dosage Form

-

Strength

8.5%;110MG/100ML;230MG/100ML;10MG/100ML;440MG/100ML;690MG/100ML

Approval Date

1988-07-01

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 0.8MG BASE/ML

Approval Date

1987-08-28

62814 / 1 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

1

Dosage Form

-

Strength

EQ 0.8MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1987-08-28

62814 / 2 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

2

Dosage Form

-

Strength

EQ 1.2MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 1.4MG BASE/ML

Approval Date

1987-08-28

62814 / 3 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

3

Dosage Form

-

Strength

EQ 1.4MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1987-08-28

62814 / 4 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

4

Dosage Form

-

Strength

EQ 1.6MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

EQ 1.8MG BASE/ML

Approval Date

1987-08-28

62814 / 5 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

5

Dosage Form

-

Strength

EQ 1.8MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1987-08-28

62814 / 6 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

6

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

EQ 2.4MG BASE/ML

Approval Date

1987-08-28

62814 / 7 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

7

Dosage Form

-

Strength

EQ 2.4MG BASE/ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

EQ 40MG BASE/100ML

Approval Date

1987-08-28

62814 / 8 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

8

Dosage Form

-

Strength

EQ 40MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

EQ 60MG BASE/100ML

Approval Date

1987-08-28

62814 / 9 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

9

Dosage Form

-

Strength

EQ 60MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

10

Dosage Form

-

Strength

EQ 70MG BASE/100ML

Approval Date

1987-08-28

62814 / 10 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

10

Dosage Form

-

Strength

EQ 70MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1987-08-28

62814 / 11 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

11

Dosage Form

-

Strength

EQ 80MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

12

Dosage Form

-

Strength

EQ 90MG BASE/100ML

Approval Date

1987-08-28

62814 / 12 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

12

Dosage Form

-

Strength

EQ 90MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

13

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1987-08-28

62814 / 13 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

13

Dosage Form

-

Strength

EQ 100MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1987

28 Aug

Discontinued Application: 62814

Drug Name

GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

14

Dosage Form

-

Strength

EQ 120MG BASE/100ML

Approval Date

1987-08-28

62814 / 14 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62814

Product Number

14

Dosage Form

-

Strength

EQ 120MG BASE/100ML

Approval Date

1987-08-28

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 16784

Drug Name

GLYCINE 1.5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

1.5GM/100ML

Approval Date

1982-01-01

16784 / 1 View Details

Active Ingredient

GLYCINE

Application Number

16784

Product Number

1

Dosage Form

-

Strength

1.5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1985

29 Mar

Discontinued Application: 19042

Drug Name

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

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1985-03-29

19042 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19042

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1985-03-29

Regulatory Status

Discontinued

1992

20 Jul

RX Application: 19953

Drug Name

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

Product Number

1

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1992-07-20

19953 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19953

Product Number

1

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1992-07-20

Regulatory Status

RX

1992

20 Jul

Discontinued Application: 19802

Drug Name

HEPARIN SODIUM 12,500 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

19802 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19802

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19042

Drug Name

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

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1985-03-29

19042 / 2 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19042

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1985-03-29

Regulatory Status

Discontinued

2023

15 Dec

RX Application: 19953

Drug Name

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

Product Number

2

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

2023-12-15

19953 / 2 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19953

Product Number

2

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

2023-12-15

Regulatory Status

RX

1992

20 Jul

RX Application: 19952

Drug Name

HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

4,000 UNITS/100ML

Approval Date

1992-07-20

19952 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19952

Product Number

1

Dosage Form

-

Strength

4,000 UNITS/100ML

Approval Date

1992-07-20

Regulatory Status

RX

1985

29 Mar

Discontinued Application: 19134

Drug Name

HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1985-03-29

19134 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19134

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1985-03-29

Regulatory Status

Discontinued

1992

20 Jul

RX Application: 19952

Drug Name

HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1992-07-20

19952 / 4 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19952

Product Number

4

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1992-07-20

Regulatory Status

RX

1992

20 Jul

RX Application: 19952

Drug Name

HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

10,000 UNITS/100ML

Approval Date

1992-07-20

19952 / 5 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19952

Product Number

5

Dosage Form

-

Strength

10,000 UNITS/100ML

Approval Date

1992-07-20

Regulatory Status

RX

1992

20 Jul

Discontinued Application: 19802

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

19802 / 2 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19802

Product Number

2

Dosage Form

-

Strength

10,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

Regulatory Status

Discontinued

1992

20 Jul

Discontinued Application: 19802

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

19802 / 5 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19802

Product Number

5

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

Regulatory Status

Discontinued

2025

25 Mar

RX Application: 19953

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

2025-03-25

19953 / 3 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19953

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

2025-03-25

Regulatory Status

RX

2025

25 Mar

RX Application: 19953

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

10,000 UNITS/100ML

Approval Date

2025-03-25

19953 / 4 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19953

Product Number

4

Dosage Form

-

Strength

10,000 UNITS/100ML

Approval Date

2025-03-25

Regulatory Status

RX

1985

29 Mar

Discontinued Application: 19135

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1985-03-29

19135 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19135

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/100ML

Approval Date

1985-03-29

Regulatory Status

Discontinued

1992

20 Jul

Discontinued Application: 19802

Drug Name

HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

19802 / 3 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19802

Product Number

3

Dosage Form

-

Strength

5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-07-20

Regulatory Status

Discontinued

1985

29 Mar

Discontinued Application: 19042

Drug Name

HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

1,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

19042 / 4 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

19042

Product Number

4

Dosage Form

-

Strength

1,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-03-29

Regulatory Status

Discontinued

1982

03 Aug

Discontinued Application: 18676

Drug Name

HEPATAMINE 8%

Product Number

1

Dosage Form

-

Strength

8% (8GM/100ML)

Approval Date

1982-08-03

18676 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

18676

Product Number

1

Dosage Form

-

Strength

8% (8GM/100ML)

Approval Date

1982-08-03

Regulatory Status

Discontinued

1984

10 Jan

Discontinued Application: 6170

Drug Name

HYPROTIGEN 5%

Product Number

3

Dosage Form

-

Strength

5%

Approval Date

1984-01-10

6170 / 3 View Details

Active Ingredient

PROTEIN HYDROLYSATE

Application Number

6170

Product Number

3

Dosage Form

-

Strength

5%

Approval Date

1984-01-10

Regulatory Status

Discontinued

1993

20 Dec

Discontinued Application: 19867

Drug Name

ISOLYTE E IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1993-12-20

19867 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE

Application Number

19867

Product Number

1

Dosage Form

-

Strength

35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1993-12-20

Regulatory Status

Discontinued

1983

31 Oct

Discontinued Application: 18899

Drug Name

ISOLYTE E IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1983-10-31

18899 / 1 View Details

Active Ingredient

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

Application Number

18899

Product Number

1

Dosage Form

-

Strength

35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1983-10-31

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19718

Drug Name

ISOLYTE E IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1989-09-29

19718 / 1 View Details

Active Ingredient

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

Application Number

19718

Product Number

1

Dosage Form

-

Strength

35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1983

17 Jan

Discontinued Application: 18269

Drug Name

ISOLYTE E W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1983-01-17

18269 / 2 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE

Application Number

18269

Product Number

2

Dosage Form

-

Strength

35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML

Approval Date

1983-01-17

Regulatory Status

Discontinued

1993

10 Jun

Discontinued Application: 19844

Drug Name

ISOLYTE H IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML

Approval Date

1993-06-10

19844 / 1 View Details

Active Ingredient

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

19844

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML

Approval Date

1993-06-10

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18273

Drug Name

ISOLYTE H W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML

Approval Date

1982-01-01

18273 / 1 View Details

Active Ingredient

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18273

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

10 Jun

Discontinued Application: 19870

Drug Name

ISOLYTE M IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML

Approval Date

1993-06-10

19870 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

19870

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML

Approval Date

1993-06-10

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18270

Drug Name

ISOLYTE M W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML

Approval Date

1982-01-01

18270 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE

Application Number

18270

Product Number

1

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

10 Jun

RX Application: 19873

Drug Name

ISOLYTE P IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML

Approval Date

1993-06-10

19873 / 1 View Details

Active Ingredient

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

Application Number

19873

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML

Approval Date

1993-06-10

Regulatory Status

RX

1984

27 Dec

Discontinued Application: 19025

Drug Name

ISOLYTE P W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML

Approval Date

1984-12-27

19025 / 1 View Details

Active Ingredient

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

Application Number

19025

Product Number

1

Dosage Form

-

Strength

5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML

Approval Date

1984-12-27

Regulatory Status

Discontinued

1993

10 Jun

Discontinued Application: 19864

Drug Name

ISOLYTE R IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML

Approval Date

1993-06-10

19864 / 1 View Details

Active Ingredient

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

Application Number

19864

Product Number

1

Dosage Form

-

Strength

37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML

Approval Date

1993-06-10

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18271

Drug Name

ISOLYTE R W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML

Approval Date

1982-01-01

18271 / 1 View Details

Active Ingredient

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

Application Number

18271

Product Number

1

Dosage Form

-

Strength

37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

09 Aug

Discontinued Application: 19843

Drug Name

ISOLYTE S IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1993-08-09

19843 / 1 View Details

Active Ingredient

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

Application Number

19843

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1993-08-09

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18252

Drug Name

ISOLYTE S IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1982-01-01

18252 / 1 View Details

Active Ingredient

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

Application Number

18252

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989

29 Sep

RX Application: 19711

Drug Name

ISOLYTE S IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1989-09-29

19711 / 1 View Details

Active Ingredient

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

Application Number

19711

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1989-09-29

Regulatory Status

RX

1984

04 Apr

Discontinued Application: 19006

Drug Name

ISOLYTE S PH 7.4 IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

Approval Date

1984-04-04

19006 / 1 View Details

Active Ingredient

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19006

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

Approval Date

1984-04-04

Regulatory Status

Discontinued

1989

29 Sep

RX Application: 19696

Drug Name

ISOLYTE S PH 7.4 IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

Approval Date

1989-09-29

19696 / 1 View Details

Active Ingredient

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Application Number

19696

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML

Approval Date

1989-09-29

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18274

Drug Name

ISOLYTE S W/ DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1982-01-01

18274 / 1 View Details

Active Ingredient

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

Application Number

18274

Product Number

1

Dosage Form

-

Strength

5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18023

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

18023 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18023

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

27 Dec

RX Application: 18681

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-12-27

18681 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

18681

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-12-27

Regulatory Status

RX

1988

29 Feb

RX Application: 19632

Drug Name

LACTATED RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1988-02-29

19632 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19632

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1988-02-29

Regulatory Status

RX

1984

30 Mar

Discontinued Application: 18967

Drug Name

LIDOCAINE HYDROCHLORIDE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1984-03-30

18967 / 1 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18967

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1984-03-30

Regulatory Status

Discontinued

1992

08 Apr

RX Application: 19830

Drug Name

LIDOCAINE HYDROCHLORIDE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1992-04-08

19830 / 2 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

1984

30 Mar

Discontinued Application: 18967

Drug Name

LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

400MG/100ML

Approval Date

1984-03-30

18967 / 2 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18967

Product Number

2

Dosage Form

-

Strength

400MG/100ML

Approval Date

1984-03-30

Regulatory Status

Discontinued

1992

08 Apr

RX Application: 19830

Drug Name

LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1992-04-08

19830 / 3 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

1984

30 Mar

Discontinued Application: 18967

Drug Name

LIDOCAINE HYDROCHLORIDE 0.8% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

800MG/100ML

Approval Date

1984-03-30

18967 / 3 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

18967

Product Number

3

Dosage Form

-

Strength

800MG/100ML

Approval Date

1984-03-30

Regulatory Status

Discontinued

1992

08 Apr

RX Application: 19830

Drug Name

LIDOCAINE HYDROCHLORIDE 0.8% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

800MG/100ML

Approval Date

1992-04-08

19830 / 4 View Details

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

4

Dosage Form

-

Strength

800MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 10%

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

16080 / 2 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

26 Jul

RX Application: 20006

Drug Name

MANNITOL 10% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1993-07-26

20006 / 2 View Details

Active Ingredient

MANNITOL

Application Number

20006

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER

Product Number

6

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

16080 / 6 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

6

Dosage Form

-

Strength

10GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 15%

Product Number

3

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

16080 / 3 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

3

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

26 Jul

RX Application: 20006

Drug Name

MANNITOL 15% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

15GM/100ML

Approval Date

1993-07-26

20006 / 3 View Details

Active Ingredient

MANNITOL

Application Number

20006

Product Number

3

Dosage Form

-

Strength

15GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45%

Product Number

5

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

16080 / 5 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

5

Dosage Form

-

Strength

15GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 14738

Drug Name

MANNITOL 20%

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

14738 / 1 View Details

Active Ingredient

MANNITOL

Application Number

14738

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 20%

Product Number

4

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

16080 / 4 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

4

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

26 Jul

RX Application: 20006

Drug Name

MANNITOL 20% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

20GM/100ML

Approval Date

1993-07-26

20006 / 4 View Details

Active Ingredient

MANNITOL

Application Number

20006

Product Number

4

Dosage Form

-

Strength

20GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 5%

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16080 / 1 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

26 Jul

RX Application: 20006

Drug Name

MANNITOL 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1993-07-26

20006 / 1 View Details

Active Ingredient

MANNITOL

Application Number

20006

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 16080

Drug Name

MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%

Product Number

7

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16080 / 7 View Details

Active Ingredient

MANNITOL

Application Number

16080

Product Number

7

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

31 Aug

Discontinued Application: 18674

Drug Name

METRO I.V.

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1982-08-31

18674 / 1 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18674

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1982-08-31

Regulatory Status

Discontinued

1983

29 Sep

Discontinued Application: 18900

Drug Name

METRO I.V. IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1983-09-29

18900 / 1 View Details

Active Ingredient

METRONIDAZOLE

Application Number

18900

Product Number

1

Dosage Form

-

Strength

500MG/100ML

Approval Date

1983-09-29

Regulatory Status

Discontinued

2004

18 Aug

Discontinued Application: 76414

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

2004-08-18

76414 / 1 View Details

Active Ingredient

MILRINONE LACTATE

Application Number

76414

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2004-08-18

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17766

Drug Name

NEPHRAMINE 5.4%

Product Number

1

Dosage Form

-

Strength

5.4% (5.4GM/100ML)

Approval Date

1982-01-01

17766 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

17766

Product Number

1

Dosage Form

-

Strength

5.4% (5.4GM/100ML)

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993

28 May

Discontinued Application: 19531

Drug Name

NUTRILIPID 10%

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1993-05-28

19531 / 1 View Details

Active Ingredient

SOYBEAN OIL

Application Number

19531

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1993-05-28

Regulatory Status

Discontinued

1993

28 May

RX Application: 19531

Drug Name

NUTRILIPID 20%

Product Number

2

Dosage Form

-

Strength

20%

Approval Date

1993-05-28

19531 / 2 View Details

Active Ingredient

SOYBEAN OIL

Application Number

19531

Product Number

2

Dosage Form

-

Strength

20%

Approval Date

1993-05-28

Regulatory Status

RX

1984

08 Jun

RX Application: 19024

Drug Name

PHYSIOLYTE IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1984-06-08

19024 / 1 View Details

Active Ingredient

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

Application Number

19024

Product Number

1

Dosage Form

-

Strength

30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Approval Date

1984-06-08

Regulatory Status

RX

1982

01 Jan

RX Application: 85870

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

85870 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE

Application Number

85870

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

31

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 31 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

31

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

37

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 37 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

37

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

43

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 43 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

43

Dosage Form

-

Strength

10GM/100ML;37MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

1

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 7 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

7

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

13

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;330MG/100ML

Approval Date

1988-02-17

19630 / 13 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

13

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;330MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

19

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 19 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

19

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

25

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 25 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

25

Dosage Form

-

Strength

5GM/100ML;37MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1989

29 Sep

Discontinued Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;37MG/100ML

Approval Date

1989-09-29

19699 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

1

Dosage Form

-

Strength

5GM/100ML;37MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.037% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

37MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

1

Dosage Form

-

Strength

37MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

32

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 32 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

32

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

38

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 38 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

38

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

44

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 44 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

44

Dosage Form

-

Strength

10GM/100ML;75MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1992

07 May

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

49

Dosage Form

-

Strength

3.3GM/100ML;75MG/100ML;300MG/100ML

Approval Date

1992-05-07

19630 / 49 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

49

Dosage Form

-

Strength

3.3GM/100ML;75MG/100ML;300MG/100ML

Approval Date

1992-05-07

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

8

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 8 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

8

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

14

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 14 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

14

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

20

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 20 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

20

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

26

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 26 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

26

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18744

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1982-11-09

18744 / 1 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

18744

Product Number

1

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1989-09-29

19699 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

2

Dosage Form

-

Strength

5GM/100ML;75MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.075% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

75MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 2 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

2

Dosage Form

-

Strength

75MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

33

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 33 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

33

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

39

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 39 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

39

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

45

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 45 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

45

Dosage Form

-

Strength

10GM/100ML;110MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1992

07 May

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

50

Dosage Form

-

Strength

3.3GM/100ML;110MG/100ML;300MG/100ML

Approval Date

1992-05-07

19630 / 50 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

50

Dosage Form

-

Strength

3.3GM/100ML;110MG/100ML;300MG/100ML

Approval Date

1992-05-07

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

3

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

9

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 9 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

9

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

15

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;330MG/100ML

Approval Date

1988-02-17

19630 / 15 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

15

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;330MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

21

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 21 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

21

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

27

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 27 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

27

Dosage Form

-

Strength

5GM/100ML;110MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1989

29 Sep

Discontinued Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1989-09-29

19699 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

3

Dosage Form

-

Strength

5GM/100ML;110MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.11% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

110MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 3 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

3

Dosage Form

-

Strength

110MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

34

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 34 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

34

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

40

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 40 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

40

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

46

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 46 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

46

Dosage Form

-

Strength

10GM/100ML;150MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1992

07 May

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

51

Dosage Form

-

Strength

3.3GM/100ML;150MG/100ML;300MG/100ML

Approval Date

1992-05-07

19630 / 51 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

51

Dosage Form

-

Strength

3.3GM/100ML;150MG/100ML;300MG/100ML

Approval Date

1992-05-07

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 10 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

10

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

16

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 16 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

16

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

22

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 22 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

22

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

28

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 28 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

28

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18744

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1982-11-09

18744 / 2 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

18744

Product Number

2

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1989

29 Sep

RX Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1989-09-29

19699 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

4

Dosage Form

-

Strength

5GM/100ML;150MG/100ML

Approval Date

1989-09-29

Regulatory Status

RX

1989

29 Sep

RX Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 4 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

4

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

35

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 35 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

35

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

41

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 41 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

41

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

47

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 47 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

47

Dosage Form

-

Strength

10GM/100ML;220MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1992

07 May

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

52

Dosage Form

-

Strength

3.3GM/100ML;220MG/100ML;300MG/100ML

Approval Date

1992-05-07

19630 / 52 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

52

Dosage Form

-

Strength

3.3GM/100ML;220MG/100ML;300MG/100ML

Approval Date

1992-05-07

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

11

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 11 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

11

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

17

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;330MG/100ML

Approval Date

1988-02-17

19630 / 17 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

17

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;330MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

23

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 23 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

23

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

29

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 29 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

29

Dosage Form

-

Strength

5GM/100ML;220MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18744

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

5GM/100ML;220MG/100ML

Approval Date

1982-11-09

18744 / 3 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

18744

Product Number

3

Dosage Form

-

Strength

5GM/100ML;220MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML

Approval Date

1989-09-29

19699 / 5 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

5

Dosage Form

-

Strength

5GM/100ML;220MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1989

29 Sep

Discontinued Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.22% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

220MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 5 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

5

Dosage Form

-

Strength

220MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

36

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1988-02-17

19630 / 36 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

36

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;200MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

42

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1988-02-17

19630 / 42 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

42

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;450MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

48

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1988-02-17

19630 / 48 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

48

Dosage Form

-

Strength

10GM/100ML;300MG/100ML;900MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1992

07 May

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 3.3% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

53

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML;300MG/100ML

Approval Date

1992-05-07

19630 / 53 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

53

Dosage Form

-

Strength

3.3GM/100ML;300MG/100ML;300MG/100ML

Approval Date

1992-05-07

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;110MG/100ML

Approval Date

1988-02-17

19630 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML;110MG/100ML

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER

Product Number

12

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 12 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

12

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Product Number

18

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 18 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

18

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

24

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 24 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

24

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1988

17 Feb

RX Application: 19630

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

30

Dosage Form

-

Strength

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

Approval Date

1988-02-17

19630 / 30 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19630

Product Number

30

Dosage Form

-

Strength

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

Approval Date

1988-02-17

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18744

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1982-11-09

18744 / 4 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

18744

Product Number

4

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1989

29 Sep

RX Application: 19699

Drug Name

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1989-09-29

19699 / 6 View Details

Active Ingredient

DEXTROSE; POTASSIUM CHLORIDE

Application Number

19699

Product Number

6

Dosage Form

-

Strength

5GM/100ML;300MG/100ML

Approval Date

1989-09-29

Regulatory Status

RX

1989

29 Sep

Discontinued Application: 19708

Drug Name

POTASSIUM CHLORIDE 0.3% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1989-09-29

19708 / 6 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

19708

Product Number

6

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1989-09-29

Regulatory Status

Discontinued

1982

08 May

Discontinued Application: 18582

Drug Name

PROCALAMINE

Product Number

1

Dosage Form

-

Strength

3%;26MG/100ML;3GM/100ML;54MG/100ML;41MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML

Approval Date

1982-05-08

18582 / 1 View Details

Active Ingredient

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

Application Number

18582

Product Number

1

Dosage Form

-

Strength

3%;26MG/100ML;3GM/100ML;54MG/100ML;41MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML

Approval Date

1982-05-08

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16704

Drug Name

RESECTISOL

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16704 / 2 View Details

Active Ingredient

MANNITOL

Application Number

16704

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 16772

Drug Name

RESECTISOL IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

16772 / 2 View Details

Active Ingredient

MANNITOL

Application Number

16772

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 18156

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18156 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18156

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18721

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-11-09

18721 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18721

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-11-09

Regulatory Status

Discontinued

1992

17 Apr

RX Application: 20002

Drug Name

RINGERS IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1992-04-17

20002 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

20002

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1992-04-17

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 17038

Drug Name

SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

17038 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

17038

Product Number

1

Dosage Form

-

Strength

20GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18184

Drug Name

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1982-01-01

18184 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

18184

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

09 Mar

RX Application: 19635

Drug Name

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1988-03-09

19635 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19635

Product Number

1

Dosage Form

-

Strength

450MG/100ML

Approval Date

1988-03-09

Regulatory Status

RX

2016

08 Aug

RX Application: 19635

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

5

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2016-08-08

19635 / 5 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19635

Product Number

5

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2016-08-08

Regulatory Status

RX

1982

09 Nov

Discontinued Application: 18722

Drug Name

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

75MG/100ML;900MG/100ML

Approval Date

1982-11-09

18722 / 1 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18722

Product Number

1

Dosage Form

-

Strength

75MG/100ML;900MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1982

09 Nov

Discontinued Application: 18722

Drug Name

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1982-11-09

18722 / 2 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18722

Product Number

2

Dosage Form

-

Strength

150MG/100ML;900MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1982

09 Nov

Discontinued Application: 18722

Drug Name

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

220MG/100ML;900MG/100ML

Approval Date

1982-11-09

18722 / 3 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18722

Product Number

3

Dosage Form

-

Strength

220MG/100ML;900MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1982

09 Nov

Discontinued Application: 18722

Drug Name

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1982-11-09

18722 / 4 View Details

Active Ingredient

POTASSIUM CHLORIDE; SODIUM CHLORIDE

Application Number

18722

Product Number

4

Dosage Form

-

Strength

300MG/100ML;900MG/100ML

Approval Date

1982-11-09

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 16733

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

16733 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

16733

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1982

01 Jan

RX Application: 17464

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

17464 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

17464

Product Number

1

Dosage Form

-

Strength

900MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1988

09 Mar

RX Application: 19635

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

1988-03-09

19635 / 2 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19635

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

1988-03-09

Regulatory Status

RX

1988

09 Mar

RX Application: 19635

Drug Name

SODIUM CHLORIDE 3% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

3GM/100ML

Approval Date

1988-03-09

19635 / 3 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19635

Product Number

3

Dosage Form

-

Strength

3GM/100ML

Approval Date

1988-03-09

Regulatory Status

RX

1988

09 Mar

RX Application: 19635

Drug Name

SODIUM CHLORIDE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

5GM/100ML

Approval Date

1988-03-09

19635 / 4 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

19635

Product Number

4

Dosage Form

-

Strength

5GM/100ML

Approval Date

1988-03-09

Regulatory Status

RX

1982

01 Jan

Discontinued Application: 18186

Drug Name

SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

1.87GM/100ML

Approval Date

1982-01-01

18186 / 1 View Details

Active Ingredient

SODIUM LACTATE

Application Number

18186

Product Number

1

Dosage Form

-

Strength

1.87GM/100ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992

21 Apr

Discontinued Application: 20004

Drug Name

SODIUM LACTATE 1/6 MOLAR IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

1.87GM/100ML

Approval Date

1992-04-21

20004 / 1 View Details

Active Ingredient

SODIUM LACTATE

Application Number

20004

Product Number

1

Dosage Form

-

Strength

1.87GM/100ML

Approval Date

1992-04-21

Regulatory Status

Discontinued

1982

01 Jan

RX Application: 16741

Drug Name

SORBITOL 3.3% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

3.3GM/100ML

Approval Date

1982-01-01

16741 / 1 View Details

Active Ingredient

SORBITOL

Application Number

16741

Product Number

1

Dosage Form

-

Strength

3.3GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

1984

02 Mar

Discontinued Application: 19077

Drug Name

STERILE WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1984-03-02

19077 / 1 View Details

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

19077

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1984-03-02

Regulatory Status

Discontinued

1988

29 Feb

RX Application: 19633

Drug Name

STERILE WATER FOR INJECTION IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1988-02-29

19633 / 1 View Details

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

19633

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1988-02-29

Regulatory Status

RX

1982

01 Jan

RX Application: 16734

Drug Name

STERILE WATER IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

16734 / 1 View Details

Active Ingredient

STERILE WATER FOR IRRIGATION

Application Number

16734

Product Number

1

Dosage Form

-

Strength

100%

Approval Date

1982-01-01

Regulatory Status

RX

1984

07 Nov

Discontinued Application: 19083

Drug Name

THEOPHYLLINE 0.04% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1984-11-07

19083 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19083

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.04% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1992-08-14

19826 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

1

Dosage Form

-

Strength

40MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1984

07 Nov

Discontinued Application: 19083

Drug Name

THEOPHYLLINE 0.08% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1984-11-07

19083 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19083

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.08% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1992-08-14

19826 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

2

Dosage Form

-

Strength

80MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1984

07 Nov

Discontinued Application: 19083

Drug Name

THEOPHYLLINE 0.16% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1984-11-07

19083 / 3 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19083

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.16% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1992-08-14

19826 / 3 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

3

Dosage Form

-

Strength

160MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1984

07 Nov

Discontinued Application: 19212

Drug Name

THEOPHYLLINE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1984-11-07

19212 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19212

Product Number

1

Dosage Form

-

Strength

200MG/100ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

200MG/100ML

Approval Date

1992-08-14

19826 / 4 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

4

Dosage Form

-

Strength

200MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.32% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

6

Dosage Form

-

Strength

320MG/100ML

Approval Date

1992-08-14

19826 / 6 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

6

Dosage Form

-

Strength

320MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1984

07 Nov

Discontinued Application: 19212

Drug Name

THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

400MG/100ML

Approval Date

1984-11-07

19212 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19212

Product Number

2

Dosage Form

-

Strength

400MG/100ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1984

07 Nov

Discontinued Application: 19212

Drug Name

THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

4MG/ML

Approval Date

1984-11-07

19212 / 3 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19212

Product Number

3

Dosage Form

-

Strength

4MG/ML

Approval Date

1984-11-07

Regulatory Status

Discontinued

1992

14 Aug

Discontinued Application: 19826

Drug Name

THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

5

Dosage Form

-

Strength

400MG/100ML

Approval Date

1992-08-14

19826 / 5 View Details

Active Ingredient

THEOPHYLLINE

Application Number

19826

Product Number

5

Dosage Form

-

Strength

400MG/100ML

Approval Date

1992-08-14

Regulatory Status

Discontinued

1984

20 Jul

RX Application: 19018

Drug Name

TROPHAMINE

Product Number

1

Dosage Form

-

Strength

6% (6GM/100ML)

Approval Date

1984-07-20

19018 / 1 View Details

Active Ingredient

AMINO ACIDS

Application Number

19018

Product Number

1

Dosage Form

-

Strength

6% (6GM/100ML)

Approval Date

1984-07-20

Regulatory Status

RX

1988

07 Sep

RX Application: 19018

Drug Name

TROPHAMINE 10%

Product Number

3

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1988-09-07

19018 / 3 View Details

Active Ingredient

AMINO ACIDS

Application Number

19018

Product Number

3

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1988-09-07

Regulatory Status

RX

1987

23 Dec

Discontinued Application: 19530

Drug Name

UCEPHAN

Product Number

1

Dosage Form

-

Strength

100MG/ML;100MG/ML

Approval Date

1987-12-23

19530 / 1 View Details

Active Ingredient

SODIUM BENZOATE; SODIUM PHENYLACETATE

Application Number

19530

Product Number

1

Dosage Form

-

Strength

100MG/ML;100MG/ML

Approval Date

1987-12-23

Regulatory Status

Discontinued

B. Braun Medical
FDA Approved Drugs

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FDA Approved Drug Records ( 297 records )

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B. Braun Medical FDA Approved Drugs

B. Braun Medical

Company Overview

Company Snapshot

FDA Approved Drug Records ( 297 records )

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B. Braun Medical
FDA Approved Drugs