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"68084-642-21" National Drug Code (NDC)

Voriconazole 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-642-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-642-11)
(American Health Packaging)

NDC Code68084-642-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-642-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-642-11)
Product NDC68084-642
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140107
End Marketing Date20180930
Marketing Category NameANDA
Application NumberANDA200265
ManufacturerAmerican Health Packaging
Substance NameVORICONAZOLE
Strength50
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-642-21





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