Active Ingredient: ESTRADIOL
Proprietary Name: ESTRADERM
Dosage Form; Route of Administration: SYSTEM; TRANSDERMAL
Strength: 0.05MG/24HR
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019081
Product Number: 002
Approval Date: Sep 10, 1986
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
