NDC 76282-225 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC76282-225

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077836
Marketed since
October 20, 2006
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 (3)

Package NDCDescriptionSince
76282-225-05500 TABLET, FILM COATED in 1 BOTTLE (76282-225-05)Oct 20, 2006
76282-225-18180 TABLET, FILM COATED in 1 BOTTLE (76282-225-18)Oct 20, 2006
76282-225-6060 TABLET, FILM COATED in 1 BOTTLE (76282-225-60)Oct 20, 2006

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