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Gemfibrozil - 60429-081-05 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 60429-081
Proprietary Name: Gemfibrozil
Non Proprietary Name: Gemfibrozil
Active Ingredient(s): 600    mg/1 & nbsp;   Gemfibrozil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Gemfibrozil

Product NDC: 60429-081
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074270
Marketing Category: ANDA
Start Marketing Date: 19930927

Package Information of Gemfibrozil

Package NDC: 60429-081-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (60429-081-05)

NDC Information of Gemfibrozil

NDC Code 60429-081-05
Proprietary Name Gemfibrozil
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (60429-081-05)
Product NDC 60429-081
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19930927
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
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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