Active Ingredient: FENOFIBRATE
Proprietary Name: FENOFIBRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 145MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090715
Product Number: 002
Approval Date: Apr 5, 2012
Applicant Holder Full Name: VALEANT PHARMACEUTICALS NORTH AMERICA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information