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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 016768

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ESTROVIS (QUINESTROL)
0.1MG
Marketing Status: Discontinued
Active Ingredient: QUINESTROL
Proprietary Name: ESTROVIS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N016768
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
ESTROVIS (QUINESTROL)
0.2MG
Marketing Status: Discontinued
Active Ingredient: QUINESTROL
Proprietary Name: ESTROVIS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N016768
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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