Foundation Consumer Healthcare Discontinued
FDA Approved Drugs

Foundation Consumer Healthcare 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 Jul 12, 2012
  • Data Source FDA
  • First Approval Date Jul 28, 1999
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Discontinued
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Company

Foundation Consumer Healthcare Discontinued

Country

U.S.A

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Company Snapshot

Foundation Consumer Healthcare Discontinued

Pittsburgh, PA 15205

U.S.A

foundationch.com/ View on Map
FDA Approved Drug Records ( 4 records )
2009
28 Aug
Discontinued Application: 78665

Drug Name

LEVONORGESTREL

Product Number

1

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-28

78665 / 1

Active Ingredient

LEVONORGESTREL

Application Number

78665

Product Number

1

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-08-28

Regulatory Status

Discontinued

2012
12 Jul
Discontinued Application: 200670

Drug Name

LEVONORGESTREL

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2012-07-12

200670 / 1

Active Ingredient

LEVONORGESTREL

Application Number

200670

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2012-07-12

Regulatory Status

Discontinued

1999
28 Jul
Discontinued Application: 21045

Drug Name

PLAN B

Product Number

1

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-07-28

21045 / 1

Active Ingredient

LEVONORGESTREL

Application Number

21045

Product Number

1

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-07-28

Regulatory Status

Discontinued

2006
24 Aug
Discontinued Application: 21045

Drug Name

PLAN B

Product Number

2

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-08-24

21045 / 2

Active Ingredient

LEVONORGESTREL

Application Number

21045

Product Number

2

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-08-24

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

Drug Name

LEVONORGESTREL

Application Number

78665

Product Number

1

Active Ingredient

LEVONORGESTREL

Dosage Form

-

Strength

0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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