Active Ingredient: PREDNICARBATE
Proprietary Name: PREDNICARBATE
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.1%
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A077236
Product Number: 001
Approval Date: Mar 9, 2007
Applicant Holder Full Name: FOUGERA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
