NDC 51655-143 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-143

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077836
Marketed since
August 14, 2017
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Gemfibrozil →

Package NDC codes (4)

Package NDCDescriptionSince
51655-143-2560 TABLET in 1 BOTTLE, PLASTIC (51655-143-25)Dec 6, 2022
51655-143-2690 TABLET in 1 BOTTLE, PLASTIC (51655-143-26)Aug 14, 2017
51655-143-5230 TABLET in 1 BOTTLE, PLASTIC (51655-143-52)Nov 13, 2017
51655-143-83180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83)Aug 14, 2017

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