Active Ingredient: ETHINYL ESTRADIOL; NORETHINDRONE
Proprietary Name: NORTREL 1/35-21
Dosage Form; Route of Administration: TABLET; ORAL-21
Strength: 0.035MG;1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072693
Product Number: 001
Approval Date: Feb 28, 1992
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information