"63629-7213-2" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (63629-7213-2)
(Bryant Ranch Prepack)

NDC Code63629-7213-2
Package Description90 TABLET in 1 BOTTLE (63629-7213-2)
Product NDC63629-7213
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20160209
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021656
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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