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"43386-089-31" National Drug Code (NDC)

Voriconazole 3 BLISTER PACK in 1 CARTON (43386-089-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43386-089-30)
(Lupin Pharmaceuticals,Inc.)

NDC Code43386-089-31
Package Description3 BLISTER PACK in 1 CARTON (43386-089-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43386-089-30)
Product NDC43386-089
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160524
Marketing Category NameANDA
Application NumberANDA207371
ManufacturerLupin Pharmaceuticals,Inc.
Substance NameVORICONAZOLE
Strength200
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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