"57297-361-02" National Drug Code (NDC)

Fenofibrate 500 TABLET in 1 BOTTLE (57297-361-02)
(LUPIN LIMITED)

NDC Code57297-361-02
Package Description500 TABLET in 1 BOTTLE (57297-361-02)
Product NDC57297-361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20120713
Marketing Category NameANDA
Application NumberANDA090856
ManufacturerLUPIN LIMITED
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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