Active Ingredient: CHOLINE FENOFIBRATE
Proprietary Name: FENOFIBRIC ACID
Dosage Form; Route of Administration: CAPSULE, DELAYED RELEASE; ORAL
Strength: EQ 135MG FENOFIBRIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207796
Product Number: 002
Approval Date: Feb 8, 2024
Applicant Holder Full Name: MACLEODS PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information