NDC 68462-581

fenofibrate 134 mg capsule

On the label: Glenmark Pharmaceuticals Inc., USA.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedDhar, IndiaMakes it and tests it Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
capsule, oral
Strength
134 mg
Approval
ANDA ANDA205566
On the market since
Apr 7, 2017
Package NDCs
68462-581-01
Official label
DailyMed (National Library of Medicine), updated Jan 31, 2026

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