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Gemfibrozil - 55154-8272-9 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 55154-8272
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: 55154-8272
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074256
Marketing Category: ANDA
Start Marketing Date: 19931031

Package Information of Gemfibrozil

Package NDC: 55154-8272-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-8272-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Gemfibrozil

NDC Code 55154-8272-9
Proprietary Name Gemfibrozil
Package Description 6 BLISTER PACK in 1 CARTON (55154-8272-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-8272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19931031
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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