Drugplain

NDC 69238-1260-9

Fenofibrate 48 mg/1

Fenofibrate · TABLET

No Recall History

Fenofibrate is a tablet containing fenofibrate at a strength of 48 mg/1. Manufactured by Amneal Pharmaceuticals NY LLC.

Key Facts

Brand Name
Fenofibrate
Generic Name
Fenofibrate
NDC Code (Package)
69238-1260-9
NDC Code (Product)
69238-1260
Manufacturer
Amneal Pharmaceuticals NY LLC
Strength
48 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA209951
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Marketing Start
02/15/2018

Recall History

No Recall History

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