Active Ingredient: PREDNICARBATE
Proprietary Name: DERMATOP
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019568
Product Number: 001
Approval Date: Sep 23, 1991
Applicant Holder Full Name: VALEANT PHARMACEUTICALS NORTH AMERICA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
