Drugplain

NDC 71335-1756-2

FENOFIBRATE 160 mg/1

FENOFIBRATE · TABLET

No Recall History

FENOFIBRATE is a tablet containing fenofibrate at a strength of 160 mg/1. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
FENOFIBRATE
Generic Name
FENOFIBRATE
NDC Code (Package)
71335-1756-2
NDC Code (Product)
71335-1756
Manufacturer
Bryant Ranch Prepack
Strength
160 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA213864
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Marketing Start
09/10/2020

Recall History

No Recall History

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FENOFIBRATE — All Packages

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.