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

NDC Code	0781-5667-13
Package Description	10 BLISTER PACK in 1 CARTON (0781-5667-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)
Product NDC	0781-5667
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Voriconazole
Non-Proprietary Name	Voriconazole
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20111212
Marketing Category Name	ANDA
Application Number	ANDA200265
Manufacturer	Sandoz Inc
Substance Name	VORICONAZOLE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]