Active Ingredient: ETHINYL ESTRADIOL; FERROUS FUMARATE; NORETHINDRONE ACETATE
Proprietary Name: NORLESTRIN FE 1/50
Dosage Form; Route of Administration: TABLET; ORAL-28
Strength: 0.05MG;75MG;1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016766
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS LABORATORIES DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
