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FENOFIBRATE - 0115-5522-03 - (FENOFIBRATE)

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Drug Information of FENOFIBRATE

Product NDC: 0115-5522
Proprietary Name: FENOFIBRATE
Non Proprietary Name: FENOFIBRATE
Active Ingredient(s): 160    mg/1 & nbsp;   FENOFIBRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FENOFIBRATE

Product NDC: 0115-5522
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: 0115-5522-03
Package Description: 1000 TABLET in 1 BOTTLE (0115-5522-03)

NDC Information of FENOFIBRATE

NDC Code 0115-5522-03
Proprietary Name FENOFIBRATE
Package Description 1000 TABLET in 1 BOTTLE (0115-5522-03)
Product NDC 0115-5522
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 160
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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