NDC 16571-784 – Gemfibrozil

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

Human Prescription Drug

Product NDC16571-784

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Rising Pharma Holdings, Inc.
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 (2)

Package NDCDescriptionSince
16571-784-0660 TABLET, FILM COATED in 1 BOTTLE (16571-784-06)Sep 16, 2015
16571-784-50500 TABLET, FILM COATED in 1 BOTTLE (16571-784-50)Sep 16, 2015

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