NDC 69315-290 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69315-290

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Leading Pharma, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210606
Marketed since
August 20, 2022
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (2)

Package NDCDescriptionSince
69315-290-05500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)Aug 20, 2022
69315-290-0990 TABLET, FILM COATED in 1 BOTTLE (69315-290-09)Aug 20, 2022

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