Drugplain

NDC 48433-039-20

Fenofibrate 48 mg/1

fenofibrate · TABLET, FILM COATED

No Recall History

Fenofibrate is a tablet, film coated containing fenofibrate at a strength of 48 mg/1. Manufactured by Safecor Health, LLC.

Key Facts

Brand Name
Fenofibrate
Generic Name
fenofibrate
NDC Code (Package)
48433-039-20
NDC Code (Product)
48433-039
Manufacturer
Safecor Health, LLC
Strength
48 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA202856
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Marketing Start
03/17/2026

Recall History

No Recall History

View Full Drug Page

Fenofibrate — All Packages

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