"0781-5667-13" National Drug Code (NDC)

Voriconazole 10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)
(Sandoz Inc)

NDC Code0781-5667-13
Package Description10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)
Product NDC0781-5667
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20111212
Marketing Category NameANDA
Application NumberANDA200265
ManufacturerSandoz Inc
Substance NameVORICONAZOLE
Strength50
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]

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