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: A211080
Product Number: 002
Approval Date: Aug 28, 2018
Applicant Holder Full Name: PRINSTON PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information