Active Ingredient: BETAMETHASONE BENZOATE
Proprietary Name: UTICORT
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.025%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018089
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
