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Gemfibrozil - 67046-230-30 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 67046-230
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: 67046-230
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074256
Marketing Category: ANDA
Start Marketing Date: 20100405

Package Information of Gemfibrozil

Package NDC: 67046-230-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-230-30)

NDC Information of Gemfibrozil

NDC Code 67046-230-30
Proprietary Name Gemfibrozil
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-230-30)
Product NDC 67046-230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100405
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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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