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GEMFIBROZIL - 57664-115-18 - (GEMFIBROZIL)

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Drug Information of GEMFIBROZIL

Product NDC: 57664-115
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: 57664-115
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079239
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of GEMFIBROZIL

Package NDC: 57664-115-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (57664-115-18)

NDC Information of GEMFIBROZIL

NDC Code 57664-115-18
Proprietary Name GEMFIBROZIL
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (57664-115-18)
Product NDC 57664-115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GEMFIBROZIL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
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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