NDC 71335-0051 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0051

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078012
Marketed since
March 23, 2017
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Gemfibrozil →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0051-160 TABLET in 1 BOTTLE (71335-0051-1)Oct 3, 2017
71335-0051-230 TABLET in 1 BOTTLE (71335-0051-2)Oct 3, 2017
71335-0051-3100 TABLET in 1 BOTTLE (71335-0051-3)Oct 3, 2017
71335-0051-490 TABLET in 1 BOTTLE (71335-0051-4)Oct 3, 2017
71335-0051-5180 TABLET in 1 BOTTLE (71335-0051-5)Oct 3, 2017

Other Gemfibrozil products