"50090-5158-1" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (50090-5158-1)
(A-S Medication Solutions)

NDC Code50090-5158-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE (50090-5158-1)
Product NDC50090-5158
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200131
Marketing Category NameANDA
Application NumberANDA210670
ManufacturerA-S Medication Solutions
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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