Stiefel Discontinued
FDA Approved Drugs

Stiefel 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 7
  • Latest Approval Date Aug 06, 2009
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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8
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Discontinued
7
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RX
1
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Stiefel Discontinued

Country

United Kingdom

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Stiefel Discontinued

980 Great West Road Brentford Middlesex TW8 9GS

United Kingdom

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FDA Approved Drug Records ( 7 records )
1982
01 Jan
Discontinued Application: 86170

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86170 / 1

Active Ingredient

HYDROCORTISONE

Application Number

86170

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86769

Drug Name

SCABENE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86769 / 1

Active Ingredient

LINDANE

Application Number

86769

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
08 Apr
Discontinued Application: 87940

Drug Name

SCABENE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-04-08

87940 / 1

Active Ingredient

LINDANE

Application Number

87940

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-04-08

Regulatory Status

Discontinued

1996
28 Oct
Discontinued Application: 19821

Drug Name

SORIATANE

Product Number

1

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-10-28

19821 / 1

Active Ingredient

ACITRETIN

Application Number

19821

Product Number

1

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-10-28

Regulatory Status

Discontinued

1996
28 Oct
Discontinued Application: 19821

Drug Name

SORIATANE

Product Number

2

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-10-28

19821 / 2

Active Ingredient

ACITRETIN

Application Number

19821

Product Number

2

Dosage Form

-

Strength

25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-10-28

Regulatory Status

Discontinued

2009
06 Aug
Discontinued Application: 19821

Drug Name

SORIATANE

Product Number

3

Dosage Form

-

Strength

17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-06

19821 / 3

Active Ingredient

ACITRETIN

Application Number

19821

Product Number

3

Dosage Form

-

Strength

17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-06

Regulatory Status

Discontinued

2009
06 Aug
Discontinued Application: 19821

Drug Name

SORIATANE

Product Number

4

Dosage Form

-

Strength

22.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-06

19821 / 4

Active Ingredient

ACITRETIN

Application Number

19821

Product Number

4

Dosage Form

-

Strength

22.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-06

Regulatory Status

Discontinued

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Drug Status Breakdown
7 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

HYDROCORTISONE

Application Number

86170

Product Number

1

Active Ingredient

HYDROCORTISONE

Dosage Form

-

Strength

1%

FDA Approved Drug Data

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