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Fenofibrate - 54868-5697-1 - (fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 54868-5697
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: 54868-5697
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076509
Marketing Category: ANDA
Start Marketing Date: 20061115

Package Information of Fenofibrate

Package NDC: 54868-5697-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5697-1)

NDC Information of Fenofibrate

NDC Code 54868-5697-1
Proprietary Name Fenofibrate
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5697-1)
Product NDC 54868-5697
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061115
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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