Warner Chilcott Company, LLC Unclassified
FDA Approved Drugs

Warner Chilcott Company, LLC Unclassified

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.

Unclassified
  • Total Records 1
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
94
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Unclassified
1
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Discontinued
93
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Company Overview

Company

Warner Chilcott Company, LLC Unclassified

Country

U.S.A

Email

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Company Snapshot

Warner Chilcott Company, LLC Unclassified

Administrative Headquarters Morris Corporate Center III 400 Interpace Parkway Parsippany

U.S.A

www.wcrx.com/ View on Map
FDA Approved Drug Records ( 1 record )
-
Unclassified Application: 21102

Drug Name

FEMHRT

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

-

21102 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

21102

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
1 total
  • Unclassified
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

FEMHRT

Application Number

21102

Product Number

1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Dosage Form

-

Strength

0.005MG;1MG

FDA Approved Drug Data

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