B. Braun Medical RX
FDA Approved Drugs

B. Braun Medical RX

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX
  • Total Records 129
  • Latest Approval Date Mar 25, 2025
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
297
View
Unclassified
1
View
Discontinued
167
View
RX
129
View
Company Overview

Company

B. Braun Medical RX

Country

U.S.A

Website

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Company Snapshot

B. Braun Medical RX

824 Twelfth Avenue Bethlehem, PA 18018-3524

U.S.A

www.bbraunusa.com/en.html View on Map
FDA Approved Drug Records ( 129 records )
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

Active Ingredient

ACETIC ACID, GLACIAL

Application Number

18161

Product Number

1

Dosage Form

-

Strength

250MG/100ML

Approval Date

1982-01-01

Regulatory Status

RX

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

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

Active Ingredient

AMINO ACIDS

Application Number

91112

Product Number

2

Dosage Form

-

Strength

15%(300GM/2000ML)

Approval Date

2012-04-13

Regulatory Status

RX

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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
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

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

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

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

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

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

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

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

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

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

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

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

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

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

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

2

Dosage Form

-

Strength

5GM/100ML

Approval Date

1988-02-02

Regulatory Status

RX

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

Active Ingredient

DEXTROSE

Application Number

19626

Product Number

5

Dosage Form

-

Strength

70GM/100ML

Approval Date

2015-02-18

Regulatory Status

RX

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

Active Ingredient

GLYCINE

Application Number

16784

Product Number

1

Dosage Form

-

Strength

1.5GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

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

Active Ingredient

HEPARIN SODIUM

Application Number

19953

Product Number

1

Dosage Form

-

Strength

200 UNITS/100ML

Approval Date

1992-07-20

Regulatory Status

RX

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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
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

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

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

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

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

2

Dosage Form

-

Strength

200MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

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

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

3

Dosage Form

-

Strength

400MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

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

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

19830

Product Number

4

Dosage Form

-

Strength

800MG/100ML

Approval Date

1992-04-08

Regulatory Status

RX

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

Active Ingredient

MANNITOL

Application Number

20006

Product Number

2

Dosage Form

-

Strength

10GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

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

Active Ingredient

MANNITOL

Application Number

20006

Product Number

3

Dosage Form

-

Strength

15GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

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

Active Ingredient

MANNITOL

Application Number

20006

Product Number

4

Dosage Form

-

Strength

20GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

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

Active Ingredient

MANNITOL

Application Number

20006

Product Number

1

Dosage Form

-

Strength

5GM/100ML

Approval Date

1993-07-26

Regulatory Status

RX

1993
28 May
RX Application: 19531

Drug Name

NUTRILIPID 20%

Product Number

2

Dosage Form

-

Strength

20%

Approval Date

1993-05-28

19531 / 2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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
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

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

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

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

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

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
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

Active Ingredient

SORBITOL

Application Number

16741

Product Number

1

Dosage Form

-

Strength

3.3GM/100ML

Approval Date

1982-01-01

Regulatory Status

RX

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

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

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
20 Jul
RX Application: 19018

Drug Name

TROPHAMINE

Product Number

1

Dosage Form

-

Strength

6% (6GM/100ML)

Approval Date

1984-07-20

19018 / 1

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

Active Ingredient

AMINO ACIDS

Application Number

19018

Product Number

3

Dosage Form

-

Strength

10% (10GM/100ML)

Approval Date

1988-09-07

Regulatory Status

RX

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Drug Status Breakdown
129 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ACETIC ACID 0.25% IN PLASTIC CONTAINER

Application Number

18161

Product Number

1

Active Ingredient

ACETIC ACID, GLACIAL

Dosage Form

-

Strength

250MG/100ML

FDA Approved Drug Data

Approved drug product information

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