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Gemfibrozil - 60505-0034-8 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 60505-0034
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: 60505-0034
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075034
Marketing Category: ANDA
Start Marketing Date: 19981001

Package Information of Gemfibrozil

Package NDC: 60505-0034-8
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (60505-0034-8)

NDC Information of Gemfibrozil

NDC Code 60505-0034-8
Proprietary Name Gemfibrozil
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (60505-0034-8)
Product NDC 60505-0034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19981001
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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