Active Ingredient: ETHINYL ESTRADIOL; NORETHINDRONE
Proprietary Name: NORETHINDRONE AND ETHINYL ESTRADIOL (10/11)
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.035MG,0.035MG;0.5MG,1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071043
Product Number: 001
Approval Date: Apr 1, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information