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"51079-164-03" National Drug Code (NDC)
Voriconazole 30 BLISTER PACK in 1 CARTON (51079-164-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-164-01)
(Mylan Institutional Inc.)
NDC Code
51079-164-03
Package Description
30 BLISTER PACK in 1 CARTON (51079-164-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-164-01)
Product NDC
51079-164
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Voriconazole
Non-Proprietary Name
Voriconazole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110808
End Marketing Date
20241231
Marketing Category Name
ANDA
Application Number
ANDA090547
Manufacturer
Mylan Institutional Inc.
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/51079-164-03