"51079-164-03" National Drug Code (NDC)

Voriconazole 30 BLISTER PACK in 1 CARTON (51079-164-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-164-01)
(Mylan Institutional Inc.)

NDC Code51079-164-03
Package Description30 BLISTER PACK in 1 CARTON (51079-164-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-164-01)
Product NDC51079-164
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110808
End Marketing Date20241231
Marketing Category NameANDA
Application NumberANDA090547
ManufacturerMylan Institutional 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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