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Fenofibrate - 0093-2060-98 - (Fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 0093-2060
Proprietary Name: Fenofibrate
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 145    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 0093-2060
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021656
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20041105

Package Information of Fenofibrate

Package NDC: 0093-2060-98
Package Description: 90 TABLET in 1 BOTTLE (0093-2060-98)

NDC Information of Fenofibrate

NDC Code 0093-2060-98
Proprietary Name Fenofibrate
Package Description 90 TABLET in 1 BOTTLE (0093-2060-98)
Product NDC 0093-2060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041105
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FENOFIBRATE
Strength Number 145
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


General Information