"63739-707-33" National Drug Code (NDC)

Voriconazole 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-707-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-707-33
Package Description3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-707-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC63739-707
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20111212
Marketing Category NameANDA
Application NumberANDA200265
ManufacturerMcKesson Corporation dba SKY Packaging
Substance NameVORICONAZOLE
Strength200
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]

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