"0179-0091-80" National Drug Code (NDC)

Fenofibrate 2160 TABLET in 1 BOTTLE (0179-0091-80)
(KAISER FOUNDATION HOSPITALS)

NDC Code0179-0091-80
Package Description2160 TABLET in 1 BOTTLE (0179-0091-80)
Product NDC0179-0091
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20110426
End Marketing Date20191231
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerKAISER FOUNDATION HOSPITALS
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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