Fresenius Kabi AB Brunna Discontinued
FDA Approved Drugs

Fresenius Kabi AB Brunna Discontinued

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
  • Total Records 18
  • Latest Approval Date Aug 07, 2009
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
34
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Discontinued
18
View
RX
16
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Company Overview

Company

Fresenius Kabi AB Brunna Discontinued

Country

Sweden

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Company Snapshot

Fresenius Kabi AB Brunna Discontinued

North Stockholm, Brunna

Sweden

cmo.fresenius-kabi.com/brunna-sweden View on Map
FDA Approved Drug Records ( 18 records )
2003
20 Feb
Discontinued Application: 75766

Drug Name

CALCITRIOL

Product Number

1

Dosage Form

-

Strength

0.001MG/ML

Approval Date

2003-02-20

75766 / 1

Active Ingredient

CALCITRIOL

Application Number

75766

Product Number

1

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

2

Dosage Form

-

Strength

0.002MG/ML

Approval Date

2003-02-20

75766 / 2

Active Ingredient

CALCITRIOL

Application Number

75766

Product Number

2

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

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18379 / 2

Active Ingredient

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

Application Number

18379

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18379

Drug Name

DELFLEX W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18379 / 3

Active Ingredient

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

Application Number

18379

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988
24 Jun
Discontinued Application: 18379

Drug Name

DELFLEX W/ DEXTROSE 3.5% IN PLASTIC CONTAINER

Product Number

7

Dosage Form

-

Strength

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

Approval Date

1988-06-24

18379 / 7

Active Ingredient

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

Application Number

18379

Product Number

7

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

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

18379 / 1

Active Ingredient

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

Application Number

18379

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
07 Jul
Discontinued Application: 18379

Drug Name

DELFLEX-LM W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-07-07

18379 / 4

Active Ingredient

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

Application Number

18379

Product Number

4

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

5

Dosage Form

-

Strength

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

Approval Date

1982-07-07

18379 / 5

Active Ingredient

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

Application Number

18379

Product Number

5

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

8

Dosage Form

-

Strength

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

Approval Date

1988-06-24

18379 / 8

Active Ingredient

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

Application Number

18379

Product Number

8

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

6

Dosage Form

-

Strength

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

Approval Date

1982-07-07

18379 / 6

Active Ingredient

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

Application Number

18379

Product Number

6

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

1

Dosage Form

-

Strength

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

Approval Date

1986-03-26

19395 / 1

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

1

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

2

Dosage Form

-

Strength

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

Approval Date

1986-03-26

19395 / 2

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

2

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

3

Dosage Form

-

Strength

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

Approval Date

1986-03-26

19395 / 3

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; SODIUM CHLORIDE; SODIUM LACTATE

Application Number

19395

Product Number

3

Dosage Form

-

Strength

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

Approval Date

1986-03-26

Regulatory Status

Discontinued

2008
14 May
Discontinued Application: 78606

Drug Name

MITOXANTRONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2008-05-14

78606 / 1

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

1

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

2

Dosage Form

-

Strength

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

Approval Date

2008-05-14

78606 / 2

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

2

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

3

Dosage Form

-

Strength

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

Approval Date

2008-05-14

78606 / 3

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

78606

Product Number

3

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

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2009-08-07

78810 / 1

Active Ingredient

OXALIPLATIN

Application Number

78810

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2009-08-07

Regulatory Status

Discontinued

2009
07 Aug
Discontinued Application: 78810

Drug Name

OXALIPLATIN

Product Number

2

Dosage Form

-

Strength

100MG/VIAL

Approval Date

2009-08-07

78810 / 2

Active Ingredient

OXALIPLATIN

Application Number

78810

Product Number

2

Dosage Form

-

Strength

100MG/VIAL

Approval Date

2009-08-07

Regulatory Status

Discontinued

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Drug Status Breakdown
18 total
  • Discontinued
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

CALCITRIOL

Application Number

75766

Product Number

1

Active Ingredient

CALCITRIOL

Dosage Form

-

Strength

0.001MG/ML

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