"69238-1263-9" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (69238-1263-9)
(Amneal Pharmaceuticals NY LLC)

NDC Code69238-1263-9
Package Description90 TABLET in 1 BOTTLE (69238-1263-9)
Product NDC69238-1263
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180323
Marketing Category NameANDA
Application NumberANDA209950
ManufacturerAmneal Pharmaceuticals NY LLC
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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