"68382-736-05" National Drug Code (NDC)

Voriconazole 500 TABLET in 1 BOTTLE (68382-736-05)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-736-05
Package Description500 TABLET in 1 BOTTLE (68382-736-05)
Product NDC68382-736
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormTABLET
UsageORAL
Start Marketing Date20160525
End Marketing Date20200801
Marketing Category NameANDA
Application NumberANDA206747
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameVORICONAZOLE
Strength200
Strength Unitmg/1
Pharmacy ClassesAzole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]

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