Leo Pharma Discontinued
FDA Approved Drugs

Leo Pharma 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 4
  • Latest Approval Date Jan 23, 2012
  • Data Source FDA
  • First Approval Date Jul 14, 2000
All
16
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Unclassified
2
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Discontinued
4
View
RX
10
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Company Overview

Company

Leo Pharma Discontinued

Country

Denmark

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Company Snapshot

Leo Pharma Discontinued

Industriparken 55

Denmark

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FDA Approved Drug Records ( 4 records )
2006
20 Oct
Discontinued Application: 21844

Drug Name

DESONATE

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-10-20

21844 / 1

Active Ingredient

DESONIDE

Application Number

21844

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-10-20

Regulatory Status

Discontinued

2000
14 Jul
Discontinued Application: 20484

Drug Name

INNOHEP

Product Number

1

Dosage Form

-

Strength

20,000 IU/ML

Approval Date

2000-07-14

20484 / 1

Active Ingredient

TINZAPARIN SODIUM

Application Number

20484

Product Number

1

Dosage Form

-

Strength

20,000 IU/ML

Approval Date

2000-07-14

Regulatory Status

Discontinued

2012
23 Jan
Discontinued Application: 202833

Drug Name

PICATO

Product Number

1

Dosage Form

-

Strength

0.015%

Approval Date

2012-01-23

202833 / 1

Active Ingredient

INGENOL MEBUTATE

Application Number

202833

Product Number

1

Dosage Form

-

Strength

0.015%

Approval Date

2012-01-23

Regulatory Status

Discontinued

2012
23 Jan
Discontinued Application: 202833

Drug Name

PICATO

Product Number

2

Dosage Form

-

Strength

0.05%

Approval Date

2012-01-23

202833 / 2

Active Ingredient

INGENOL MEBUTATE

Application Number

202833

Product Number

2

Dosage Form

-

Strength

0.05%

Approval Date

2012-01-23

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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

DESONATE

Application Number

21844

Product Number

1

Active Ingredient

DESONIDE

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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