BASF
FDA Approved Drugs

BASF

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 6
  • Latest Approval Date Jul 23, 1986
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

BASF

Country

Germany

Website

Visit Website

Email

global.info@basf.com

Social Profiles

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Company Snapshot

BASF

Carl-Bosch-Strasse 38 Ludwigshafen , Rhineland-Palatinate 67056

Germany

pharmaceutical.basf.com/global/en.html global.info@basf.com View on Map
FDA Approved Drug Records ( 6 records )
1982
01 Jan
Discontinued Application: 18197

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

18197 / 1

Active Ingredient

IBUPROFEN

Application Number

18197

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
22 Feb
Discontinued Application: 70083

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1985-02-22

70083 / 1

Active Ingredient

IBUPROFEN

Application Number

70083

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1985-02-22

Regulatory Status

Discontinued

1985
08 Feb
Discontinued Application: 70088

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-02-08

70088 / 1

Active Ingredient

IBUPROFEN

Application Number

70088

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-02-08

Regulatory Status

Discontinued

1985
29 Mar
Discontinued Application: 70099

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-03-29

70099 / 1

Active Ingredient

IBUPROFEN

Application Number

70099

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1985-03-29

Regulatory Status

Discontinued

1986
23 Jul
Discontinued Application: 70745

Drug Name

IBU

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1986-07-23

70745 / 1

Active Ingredient

IBUPROFEN

Application Number

70745

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

1986-07-23

Regulatory Status

Discontinued

1984
05 Mar
Discontinued Application: 18197

Drug Name

RUFEN

Product Number

2

Dosage Form

-

Strength

600MG

Approval Date

1984-03-05

18197 / 2

Active Ingredient

IBUPROFEN

Application Number

18197

Product Number

2

Dosage Form

-

Strength

600MG

Approval Date

1984-03-05

Regulatory Status

Discontinued

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Drug Status Breakdown
6 total
  • Discontinued
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

IBU

Application Number

18197

Product Number

1

Active Ingredient

IBUPROFEN

Dosage Form

-

Strength

400MG

FDA Approved Drug Data

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