NDC 63629-9474

Fenofibrate 160 mg tablet, film coated

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack 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, oral
Strength
160 mg
Approval
ANDA ANDA076433
On the market since
Jun 1, 2017
Package NDCs
63629-9474-1
Official label
DailyMed (National Library of Medicine), updated Jan 12, 2024

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