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: A200884
Product Number: 002
Approval Date: Sep 7, 2017
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information