"50268-804-12" National Drug Code (NDC)

NDC Code	50268-804-12
Package Description	20 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-804-12) > 1 TABLET in 1 BLISTER PACK (50268-804-11)
Product NDC	50268-804
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Voriconazole
Non-Proprietary Name	Voriconazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20161207
Marketing Category Name	ANDA
Application Number	ANDA206747
Manufacturer	AvPAK
Substance Name	VORICONAZOLE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]