Fresenius Kabi AB Brunna
FDA Approved Drugs

Fresenius Kabi AB Brunna

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.

Discontinued RX

Total Records 34
Latest Approval Date May 18, 2018
Data Source FDA
First Approval Date Jan 01, 1982

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Discontinued

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Company Overview

Company

Fresenius Kabi AB Brunna

Country

Sweden

Website

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Company Snapshot

Fresenius Kabi AB Brunna

North Stockholm, Brunna

Sweden

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FDA Approved Drug Records ( 34 records )

2003

20 Feb

Discontinued Application: 75766

Drug Name

CALCITRIOL

Product Number

Dosage Form

Strength

0.001MG/ML

Approval Date

2003-02-20

75766 / 1 View Details

Active Ingredient

CALCITRIOL

Application Number

75766

Product Number

Dosage Form

Strength

0.001MG/ML

Approval Date

2003-02-20

Regulatory Status

Discontinued

2003

20 Feb

Discontinued Application: 75766

Drug Name

CALCITRIOL

Product Number

Dosage Form

Strength

0.002MG/ML

Approval Date

2003-02-20

75766 / 2 View Details

Active Ingredient

CALCITRIOL

Application Number

75766

Product Number

Dosage Form

Strength

0.002MG/ML

Approval Date

2003-02-20

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18379

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

1982-01-01

18379 / 2 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

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

1982

01 Jan

Discontinued Application: 18379

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

1982-01-01

18379 / 3 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

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

1988

24 Jun

Discontinued Application: 18379

Drug Name

DELFLEX W/ DEXTROSE 3.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;3.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1988-06-24

18379 / 7 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

25.7MG/100ML;3.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Approval Date

1988-06-24

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 18379

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

1982-01-01

18379 / 1 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

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

1982

07 Jul

Discontinued Application: 18379

Drug Name

DELFLEX-LM W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

18379 / 4 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

Regulatory Status

Discontinued

1982

07 Jul

Discontinued Application: 18379

Drug Name

DELFLEX-LM W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

18379 / 5 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

Regulatory Status

Discontinued

1988

24 Jun

Discontinued Application: 18379

Drug Name

DELFLEX-LM W/ DEXTROSE 3.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

25.7MG/100ML;3.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1988-06-24

18379 / 8 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

25.7MG/100ML;3.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Approval Date

1988-06-24

Regulatory Status

Discontinued

1982

07 Jul

Discontinued Application: 18379

Drug Name

DELFLEX-LM W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

18379 / 6 View Details

Active Ingredient

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

Application Number

18379

Product Number

Dosage Form

Strength

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

Approval Date

1982-07-07

Regulatory Status

Discontinued

1986

26 Mar

Discontinued Application: 19395

Drug Name

INPERSOL-ZM W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

19395 / 1 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

Regulatory Status

Discontinued

1986

26 Mar

Discontinued Application: 19395

Drug Name

INPERSOL-ZM W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

19395 / 2 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

Regulatory Status

Discontinued

1986

26 Mar

Discontinued Application: 19395

Drug Name

INPERSOL-ZM W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

19395 / 3 View Details

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

Dosage Form

Strength

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

Approval Date

1986-03-26

Regulatory Status

Discontinued

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

2008

14 May

Discontinued Application: 78606

Drug Name

MITOXANTRONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 20MG BASE/10ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

78606 / 1 View Details

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

Dosage Form

Strength

EQ 20MG BASE/10ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

Regulatory Status

Discontinued

2008

14 May

Discontinued Application: 78606

Drug Name

MITOXANTRONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

78606 / 2 View Details

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

Dosage Form

Strength

EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

Regulatory Status

Discontinued

2008

14 May

Discontinued Application: 78606

Drug Name

MITOXANTRONE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 30MG BASE/15ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

78606 / 3 View Details

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

Dosage Form

Strength

EQ 30MG BASE/15ML (EQ 2MG BASE/ML)

Approval Date

2008-05-14

Regulatory Status

Discontinued

2009

07 Aug

Discontinued Application: 78810

Drug Name

OXALIPLATIN

Product Number

Dosage Form

Strength

50MG/VIAL

Approval Date

2009-08-07

78810 / 1 View Details

Active Ingredient

OXALIPLATIN

Application Number

78810

Product Number

Dosage Form

Strength

50MG/VIAL

Approval Date

2009-08-07

Regulatory Status

Discontinued

2009

07 Aug

Discontinued Application: 78810

Drug Name

OXALIPLATIN

Product Number

Dosage Form

Strength

100MG/VIAL

Approval Date

2009-08-07

78810 / 2 View Details

Active Ingredient

OXALIPLATIN

Application Number

78810

Product Number

Dosage Form

Strength

100MG/VIAL

Approval Date

2009-08-07

Regulatory Status

Discontinued

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

34 total

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

Drug Name

CALCITRIOL

Application Number

75766

Product Number

Active Ingredient

CALCITRIOL

Dosage Form

Strength

0.001MG/ML

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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