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"59762-0935-3" National Drug Code (NDC)
Voriconazole 1 BOTTLE in 1 CARTON (59762-0935-3) / 75 mL in 1 BOTTLE
(Greenstone LLC)
NDC Code
59762-0935-3
Package Description
1 BOTTLE in 1 CARTON (59762-0935-3) / 75 mL in 1 BOTTLE
Product NDC
59762-0935
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Voriconazole
Non-Proprietary Name
Voriconazole
Dosage Form
POWDER, FOR SUSPENSION
Usage
ORAL
Start Marketing Date
20131216
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA021630
Manufacturer
Greenstone LLC
Substance Name
VORICONAZOLE
Strength
40
Strength Unit
mg/mL
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/59762-0935-3