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Fenofibrate - 51079-599-20 - (fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 51079-599
Proprietary Name: Fenofibrate
Non Proprietary Name: fenofibrate
Active Ingredient(s): 48    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 51079-599
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202856
Marketing Category: ANDA
Start Marketing Date: 20130610

Package Information of Fenofibrate

Package NDC: 51079-599-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-599-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-599-01)

NDC Information of Fenofibrate

NDC Code 51079-599-20
Proprietary Name Fenofibrate
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-599-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-599-01)
Product NDC 51079-599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130610
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name FENOFIBRATE
Strength Number 48
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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