NDC 51655-856 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-856

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
February 13, 2023
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
51655-856-5230 TABLET in 1 BOTTLE, PLASTIC (51655-856-52)Feb 13, 2023

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