Active Ingredient: ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
Proprietary Name: NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.02MG;1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A208639
Product Number: 001
Approval Date: Mar 21, 2018
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Discontinued
Patent and Exclusivity Information