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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 206969

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL (ETHINYL ESTRADIOL; NORETHINDRONE ACETATE)
0.02MG;1MG
Marketing Status: Prescription
Active Ingredient: ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
Proprietary Name: NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.02MG;1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A206969
Product Number: 001
Approval Date: Jan 20, 2016
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
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