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"63739-008-33" National Drug Code (NDC)
Voriconazole 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-008-33) / 10 TABLET in 1 BLISTER PACK
(Mckesson Corporation DBA SKY Packaginng)
NDC Code
63739-008-33
Package Description
3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-008-33) / 10 TABLET in 1 BLISTER PACK
Product NDC
63739-008
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Voriconazole
Non-Proprietary Name
Voriconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160531
Marketing Category Name
ANDA
Application Number
ANDA206181
Manufacturer
Mckesson Corporation DBA SKY Packaginng
Substance Name
VORICONAZOLE
Strength
200
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]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-008-33