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"68462-572-13" National Drug Code (NDC)

Voriconazole 3 BLISTER PACK in 1 CARTON (68462-572-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-572-13
Package Description3 BLISTER PACK in 1 CARTON (68462-572-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC68462-572
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150904
Marketing Category NameANDA
Application NumberANDA203503
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameVORICONAZOLE
Strength50
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]

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