Active Ingredient: BETAMETHASONE DIPROPIONATE
Proprietary Name: BETAMETHASONE DIPROPIONATE
Dosage Form; Route of Administration: OINTMENT, AUGMENTED; TOPICAL
Strength: EQ 0.05% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075373
Product Number: 001
Approval Date: Jun 22, 1999
Applicant Holder Full Name: FOUGERA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
