NDC 0615-8354 – Gemfibrozil

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

Human Prescription Drug

Product NDC0615-8354

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202726
Marketed since
September 16, 2015
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 (1)

Package NDCDescriptionSince
0615-8354-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8354-39)Nov 10, 2020

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