Fresenius Kabi AB Brunna RX
FDA Approved Drugs

Fresenius Kabi AB Brunna 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.

Total Records 16
Latest Approval Date May 18, 2018
Data Source FDA
First Approval Date Nov 30, 1984

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Company

Fresenius Kabi AB Brunna RX

Country

Sweden

Website

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Company Snapshot

Fresenius Kabi AB Brunna RX

North Stockholm, Brunna

Sweden

cmo.fresenius-kabi.com/brunna-sweden View on Map

FDA Approved Drug Records ( 16 records )

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

18883 / 1 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

Regulatory Status

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 1.5% LOW MAGNESIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

18883 / 4 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

Regulatory Status

1992

19 Aug

RX Application: 20171

Drug Name

DELFLEX W/ DEXTROSE 1.5% LOW MAGNESIUM LOW CALCIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

18.4MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

20171 / 1 View Details

Active Ingredient

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

Application Number

20171

Product Number

Dosage Form

Strength

18.4MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

Regulatory Status

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

18883 / 2 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

Regulatory Status

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 2.5% LOW MAGNESIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

18883 / 5 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

Regulatory Status

1992

19 Aug

RX Application: 20171

Drug Name

DELFLEX W/ DEXTROSE 2.5% LOW MAGNESIUM LOW CALCIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

18.4MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

20171 / 2 View Details

Active Ingredient

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

Application Number

20171

Product Number

Dosage Form

Strength

18.4MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

Regulatory Status

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

18883 / 3 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1984-11-30

Regulatory Status

1984

30 Nov

RX Application: 18883

Drug Name

DELFLEX W/ DEXTROSE 4.25% LOW MAGNESIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

18883 / 6 View Details

Active Ingredient

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

Application Number

18883

Product Number

Dosage Form

Strength

25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1984-11-30

Regulatory Status

1992

19 Aug

RX Application: 20171

Drug Name

DELFLEX W/ DEXTROSE 4.25% LOW MAGNESIUM LOW CALCIUM IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

18.4MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

20171 / 3 View Details

Active Ingredient

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

Application Number

20171

Product Number

Dosage Form

Strength

18.4MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1992-08-19

Regulatory Status

2012

25 Jan

RX Application: 90502

Drug Name

LACTULOSE

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

2012-01-25

90502 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

90502

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

2012-01-25

Regulatory Status

2012

25 Jan

RX Application: 90503

Drug Name

LACTULOSE

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

2012-01-25

90503 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

90503

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

2012-01-25

Regulatory Status

2018

18 May

RX Application: 203719

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL

Approval Date

2018-05-18

203719 / 1 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

203719

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL

Approval Date

2018-05-18

Regulatory Status

2018

18 May

RX Application: 203719

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

Dosage Form

Strength

EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL

Approval Date

2018-05-18

203719 / 2 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

203719

Product Number

Dosage Form

Strength

EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL

Approval Date

2018-05-18

Regulatory Status

2018

18 May

RX Application: 203719

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

Dosage Form

Strength

EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2018-05-18

203719 / 3 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

203719

Product Number

Dosage Form

Strength

EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2018-05-18

Regulatory Status

2018

11 May

RX Application: 203720

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

Dosage Form

Strength

EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL

Approval Date

2018-05-11

203720 / 1 View Details

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

203720

Product Number

Dosage Form

Strength

EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL

Approval Date

2018-05-11

Regulatory Status

2007

12 Apr

RX Application: 78177

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

900MG/100ML

Approval Date

2007-04-12

78177 / 1 View Details

Active Ingredient

SODIUM CHLORIDE

Application Number

78177

Product Number

Dosage Form

Strength

900MG/100ML

Approval Date

2007-04-12

Regulatory Status

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Drug Status Breakdown

16 total

Official Source

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

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Drug Name

DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Application Number

18883

Product Number

Active Ingredient

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

Dosage Form

Strength

25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

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