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FENOFIBRATE - 0115-5511-01 - (FENOFIBRATE)

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Drug Information of FENOFIBRATE

Product NDC: 0115-5511
Proprietary Name: FENOFIBRATE
Non Proprietary Name: FENOFIBRATE
Active Ingredient(s): 54    mg/1 & nbsp;   FENOFIBRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FENOFIBRATE

Product NDC: 0115-5511
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076509
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of FENOFIBRATE

Package NDC: 0115-5511-01
Package Description: 100 TABLET in 1 BOTTLE (0115-5511-01)

NDC Information of FENOFIBRATE

NDC Code 0115-5511-01
Proprietary Name FENOFIBRATE
Package Description 100 TABLET in 1 BOTTLE (0115-5511-01)
Product NDC 0115-5511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENOFIBRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name FENOFIBRATE
Strength Number 54
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 FENOFIBRATE


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