NDC 0115-5522

Fenofibrate 160 mg tablet

On the label: Amneal Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals of New York, LLCBrookhaven, NY, United StatesMakes it, tests it, packages it and labels it No problems foundSep 25, 2026 · 14 inspections
Reed-Lane, Inc.Wayne, NJ, United StatesPackages it No problems foundOct 17, 2025 · 7 inspections

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, oral
Strength
160 mg
Approval
ANDA ANDA076509
On the market since
Feb 1, 2010
Package NDCs
0115-5522-01 0115-5522-02 0115-5522-03 0115-5522-10
Official label
DailyMed (National Library of Medicine), updated Apr 1, 2021

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?