NDC 59651-575

Fenofibrate 54 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, film coated, oral
Strength
54 mg
Approval
ANDA ANDA216798
On the market since
Sep 27, 2022
Package NDCs
59651-575-90
Official label
DailyMed (National Library of Medicine), updated Feb 12, 2025

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