Active Ingredient: ESTRADIOL; NORETHINDRONE ACETATE
Proprietary Name: ESTRADIOL AND NORETHINDRONE ACETATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG;0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078324
Product Number: 002
Approval Date: Jun 9, 2011
Applicant Holder Full Name: BRECKENRIDGE PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: ESTRADIOL; NORETHINDRONE ACETATE
Proprietary Name: ESTRADIOL AND NORETHINDRONE ACETATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG;0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078324
Product Number: 001
Approval Date: Apr 17, 2008
Applicant Holder Full Name: BRECKENRIDGE PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information