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Gemfibrozil - 0615-3559-39 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 0615-3559
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: 0615-3559
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074256
Marketing Category: ANDA
Start Marketing Date: 19931124

Package Information of Gemfibrozil

Package NDC: 0615-3559-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-39)

NDC Information of Gemfibrozil

NDC Code 0615-3559-39
Proprietary Name Gemfibrozil
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-39)
Product NDC 0615-3559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19931124
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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