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"0781-5668-31" National Drug Code (NDC)
Voriconazole 30 TABLET, FILM COATED in 1 BOTTLE (0781-5668-31)
(Sandoz Inc)
NDC Code
0781-5668-31
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (0781-5668-31)
Product NDC
0781-5668
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
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/0781-5668-31