NDC 35561-249 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC35561-249

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bostal LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208476
Marketed since
January 1, 2021
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 (4)

Package NDCDescriptionSince
35561-249-03500 TABLET, FILM COATED in 1 BOTTLE (35561-249-03)Aug 7, 2025
35561-249-1030 TABLET, FILM COATED in 1 BOTTLE (35561-249-10)Jan 1, 2021
35561-249-1190 TABLET, FILM COATED in 1 BOTTLE (35561-249-11)Aug 15, 2025
35561-249-13500 TABLET, FILM COATED in 1 BOTTLE (35561-249-13)Jan 1, 2021

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