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"68462-572-90" National Drug Code (NDC)
Voriconazole 90 TABLET, FILM COATED in 1 BOTTLE (68462-572-90)
(Glenmark Pharmaceuticals Inc., USA)
NDC Code
68462-572-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (68462-572-90)
Product NDC
68462-572
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Voriconazole
Non-Proprietary Name
Voriconazole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150904
Marketing Category Name
ANDA
Application Number
ANDA203503
Manufacturer
Glenmark Pharmaceuticals Inc., USA
Substance Name
VORICONAZOLE
Strength
50
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/68462-572-90