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Gemfibrozil - 0179-0037-01 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 0179-0037
Proprietary Name: Gemfibrozil
Non Proprietary Name: Gemfibrozil
Active Ingredient(s): 600    mg/1 & nbsp;   Gemfibrozil
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Gemfibrozil

Product NDC: 0179-0037
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077836
Marketing Category: ANDA
Start Marketing Date: 20091030

Package Information of Gemfibrozil

Package NDC: 0179-0037-01
Package Description: 100 TABLET, COATED in 1 BOTTLE (0179-0037-01)

NDC Information of Gemfibrozil

NDC Code 0179-0037-01
Proprietary Name Gemfibrozil
Package Description 100 TABLET, COATED in 1 BOTTLE (0179-0037-01)
Product NDC 0179-0037
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20091030
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name GEMFIBROZIL
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Complete Information of Gemfibrozil


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