Active Ingredient: ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE
Proprietary Name: ZOVIA 1/50E-21
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.05MG;1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072722
Product Number: 001
Approval Date: Dec 30, 1991
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
