"72162-2470-9" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (72162-2470-9)
(Bryant Ranch Prepack)

NDC Code72162-2470-9
Package Description90 TABLET in 1 BOTTLE (72162-2470-9)
Product NDC72162-2470
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230907
Marketing Category NameANDA
Application NumberANDA217732
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength120
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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