Active Ingredient: BETAMETHASONE DIPROPIONATE
Proprietary Name: BETAMETHASONE DIPROPIONATE
Dosage Form; Route of Administration: GEL, AUGMENTED; TOPICAL
Strength: EQ 0.05% BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A075276
Product Number: 001
Approval Date: May 13, 2003
Applicant Holder Full Name: FOUGERA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information