NDC 33342-295

Fenofibric acid 135 mg capsule, delayed release

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
capsule, delayed release, oral
Strength
135 mg
Approval
ANDA ANDA207796
On the market since
Feb 26, 2024
Package NDCs
33342-295-10 33342-295-56
Official label
DailyMed (National Library of Medicine), updated Jul 3, 2025

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