NDC 71610-824 – Gemfibrozil

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

Human Prescription Drug

Product NDC71610-824

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078012
Marketed since
April 1, 2011
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 (4)

Package NDCDescriptionSince
71610-824-3030 TABLET, FILM COATED in 1 BOTTLE (71610-824-30)Apr 29, 2024
71610-824-5360 TABLET, FILM COATED in 1 BOTTLE (71610-824-53)Apr 29, 2024
71610-824-6090 TABLET, FILM COATED in 1 BOTTLE (71610-824-60)Apr 29, 2024
71610-824-80180 TABLET, FILM COATED in 1 BOTTLE (71610-824-80)Apr 29, 2024

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