NDC 62332-539

Fenofibrate 160 mg tablet, film coated

On the label: Alembic Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, film coated, oral
Strength
160 mg
Approval
ANDA ANDA209660
On the market since
Feb 12, 2019
Package NDCs
62332-539-90 62332-539-91
Official label
DailyMed (National Library of Medicine), updated Nov 16, 2021

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