NDC 63304-449 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63304-449

Product details

Brand name
Fenofibrate
Generic name
fenofibrate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200884
Marketed since
June 1, 2018
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 (3)

Package NDCDescriptionSince
63304-449-05500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)Jun 1, 2018
63304-449-3030 TABLET, FILM COATED in 1 BOTTLE (63304-449-30)Jun 1, 2018
63304-449-9090 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)Jun 1, 2018

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