"59651-575-90" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (59651-575-90)
(Aurobindo Pharma Limited)

NDC Code59651-575-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (59651-575-90)
Product NDC59651-575
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220927
Marketing Category NameANDA
Application NumberANDA216798
ManufacturerAurobindo Pharma Limited
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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