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NDC 71335-0051-01 GEMFIBROZIL 600 mg/1 Details

GEMFIBROZIL 600 mg/1

GEMFIBROZIL is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is GEMFIBROZIL.

MedlinePlus Drug Summary

Gemfibrozil is used with diet changes (restriction of cholesterol and fat intake) to reduce the amount of cholesterol and triglycerides (other fatty substances) in the blood in certain people with very high triglycerides who are at risk of pancreatic disease (conditions affecting the pancreas, a gland that produces fluid to break down food and hormones to control blood sugar). Gemfibrozil is also used in people with a combination of low high-density lipoprotein (HDL; 'good cholesterol') levels and high low-density lipoprotein (LDL; 'bad cholesterol') and triglyceride levels to reduce the risk of heart disease. Gemfibrozil is in a class of lipid-regulating medications called fibrates. It works by reducing the production of triglycerides in the liver.

Related Packages: 71335-0051-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Gemfibrozil

Product Information

NDC	71335-0051
Product ID	71335-0051_c74824ac-46e5-491b-b323-efd70f7ad63f
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	GEMFIBROZIL
Proprietary Name Suffix	n/a
Non-Proprietary Name	GEMFIBROZIL
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	600
Active Ingredient Units	mg/1
Substance Name	GEMFIBROZIL
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	PPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078012
Listing Certified Through	2024-12-31

Package

NDC 71335-0051-01 (71335005101)

Pricing Information	N/A
NDC Package Code	71335-0051-1
Billing NDC	71335005101
Package	60 TABLET in 1 BOTTLE (71335-0051-1)
Marketing Start Date	2017-10-03
NDC Exclude Flag	N