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: Yes
TE Code: AB
Application Number: A210369
Product Number: 001
Approval Date: Dec 26, 2017
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
