NDC 51407-094

Fenofibrate 160 mg tablet, film coated

On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-660.

United States: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Adare Pharmaceuticals, Inc.Vandalia, OH, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyFeb 25, 2025 · 8 inspections
Frontida BioPharm, LLCPhiladelphia, PA, United StatesMakes it, tests it and packages it No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, film coated
Strength
160 mg
Approval
ANDA ANDA076433
On the market since
May 13, 2005
Package NDCs
51407-094-90
Official label
DailyMed (National Library of Medicine), updated Jun 16, 2026

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