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: A210670
Product Number: 002
Approval Date: Sep 6, 2019
Applicant Holder Full Name: DR REDDYS LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information