NDC 35561-344 – Fenofibrate

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

Human Prescription Drug

Product NDC35561-344

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bostal LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207803
Marketed since
June 30, 2019
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 (3)

Package NDCDescriptionSince
35561-344-0021631 TABLET, FILM COATED in 1 BOX (35561-344-00)Jun 30, 2019
35561-344-1190 TABLET, FILM COATED in 1 BOTTLE (35561-344-11)Jun 30, 2019
35561-344-13500 TABLET, FILM COATED in 1 BOTTLE (35561-344-13)Jun 30, 2019

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