"71335-2413-3" National Drug Code (NDC)

Fenofibrate 28 TABLET in 1 BOTTLE (71335-2413-3)
(Bryant Ranch Prepack)

NDC Code71335-2413-3
Package Description28 TABLET in 1 BOTTLE (71335-2413-3)
Product NDC71335-2413
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20220718
Marketing Category NameANDA
Application NumberANDA211122
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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