{
"NDC": {
"NDCCode": "60687-968-21",
"PackageDescription": "30 BLISTER PACK in 1 CARTON (60687-968-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-968-11) ",
"NDC11Code": "60687-0968-21",
"ProductNDC": "60687-968",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Voriconazole",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Voriconazole",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20260827",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA206837",
"LabelerName": "American Health Packaging",
"SubstanceName": "VORICONAZOLE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-08-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260827",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}