Drugplain

NDC 62135-899-90

fenofibrate 200 mg/1

fenofibrate · CAPSULE

No Recall History

fenofibrate is a capsule containing fenofibrate at a strength of 200 mg/1. Manufactured by Chartwell RX, LLC..

Key Facts

Brand Name
fenofibrate
Generic Name
fenofibrate
NDC Code (Package)
62135-899-90
NDC Code (Product)
62135-899
Manufacturer
Chartwell RX, LLC.
Strength
200 mg/1
Dosage Form
CAPSULE
Route
ORAL
Marketing Status
Application #
ANDA211407
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Marketing Start
01/31/2024

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.