"62135-838-90" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (62135-838-90)
(Chartwell RX, LLC)

NDC Code62135-838-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (62135-838-90)
Product NDC62135-838
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190211
Marketing Category NameANDA
Application NumberANDA209660
ManufacturerChartwell RX, LLC
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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