Active Ingredient: PROGESTERONE
Proprietary Name: PROGESTASERT
Dosage Form; Route of Administration: INSERT, EXTENDED RELEASE; INTRAUTERINE
Strength: 38MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017553
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ALZA CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
