NDC 43598-910

Fenofibrate 160 mg tablet, film coated

On the label: Dr. Reddy's Laboratories Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, film coated, oral
Strength
160 mg
Approval
ANDA ANDA210670
On the market since
Jan 31, 2020
Package NDCs
43598-910-05 43598-910-90
Official label
DailyMed (National Library of Medicine), updated Mar 24, 2021

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