NDC 71335-1902 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1902

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203266
Marketed since
February 15, 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
71335-1902-160 TABLET in 1 BOTTLE (71335-1902-1)Jul 13, 2021
71335-1902-230 TABLET in 1 BOTTLE (71335-1902-2)Aug 3, 2021
71335-1902-3100 TABLET in 1 BOTTLE (71335-1902-3)Mar 10, 2022
71335-1902-490 TABLET in 1 BOTTLE (71335-1902-4)Mar 10, 2022
71335-1902-5180 TABLET in 1 BOTTLE (71335-1902-5)Sep 13, 2021

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