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"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 Code
63739-707-33
Package Description
3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-707-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
63739-707
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
McKesson Corporation dba SKY Packaging
Substance Name
VORICONAZOLE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Azole Antifungal [EPC],Azoles [CS],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/63739-707-33