NDC 68180-388

Fenofibrate 48 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

India: 3

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedSalcette, IndiaMakes it and packages it Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action
Lupin LimitedPithampur, IndiaMakes it and packages it Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action
Lupin LimitedNagpur, IndiaMakes it and packages it Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, oral
Strength
48 mg
Approval
ANDA ANDA090856
On the market since
Aug 1, 2020
Package NDCs
68180-388-09
Official label
DailyMed (National Library of Medicine), updated Nov 19, 2025

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