NDC 71205-949 – Fenofibrate

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

Human Prescription Drug

Product NDC71205-949

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207803
Marketed since
April 23, 2020
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 (6)

Package NDCDescriptionSince
71205-949-3030 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)Oct 8, 2020
71205-949-55500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)Oct 8, 2020
71205-949-6060 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)Oct 8, 2020
71205-949-72120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)Oct 8, 2020
71205-949-78180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)Oct 8, 2020
71205-949-9090 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)Oct 8, 2020

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