NDC 69315-287 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69315-287

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Leading Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211122
Marketed since
July 18, 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 (1)

Package NDCDescriptionSince
69315-287-0990 TABLET in 1 BOTTLE (69315-287-09)Jul 18, 2022

Other Fenofibrate products