"50090-3255-1" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (50090-3255-1)
(A-S Medication Solutions)

NDC Code50090-3255-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50090-3255-1)
Product NDC50090-3255
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180702
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerA-S Medication Solutions
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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