Active Ingredient: FENOFIBRATE
Proprietary Name: FENOFIBRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 160MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076433
Product Number: 002
Approval Date: May 13, 2005
Applicant Holder Full Name: RHODES PHARMACEUTICALS LP
Marketing Status:
Prescription
Patent and Exclusivity Information
