Active Ingredient: ESTRADIOL
Proprietary Name: FEMPATCH
Dosage Form; Route of Administration: FILM, EXTENDED RELEASE; TRANSDERMAL
Strength: 0.025MG/24HR
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020417
Product Number: 001
Approval Date: Dec 3, 1996
Applicant Holder Full Name: PARKE DAVIS PHARMACEUTICAL RESEARCH DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
