NDC 65862-769

Fenofibrate 145 mg tablet, 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, coated, oral
Strength
145 mg
Approval
ANDA ANDA205118
On the market since
May 5, 2016
Package NDCs
65862-769-01 65862-769-05 65862-769-10 65862-769-78 65862-769-90 65862-769-99
Official label
DailyMed (National Library of Medicine), updated Jul 28, 2025

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