Active Ingredient: BETAMETHASONE DIPROPIONATE
Proprietary Name: BETAMETHASONE DIPROPIONATE
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: EQ 0.05% BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019141
Product Number: 001
Approval Date: Sep 4, 1984
Applicant Holder Full Name: FOUGERA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
