{
"NDC": {
"NDCCode": "70860-117-26",
"PackageDescription": "10 VIAL in 1 CARTON (70860-117-26) / 1 POWDER, FOR SOLUTION in 1 VIAL (70860-117-41) ",
"NDC11Code": "70860-0117-26",
"ProductNDC": "70860-117",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nafcillin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Nafcillin Sodium",
"DosageFormName": "POWDER, FOR SOLUTION",
"RouteName": "INTRAMUSCULAR; INTRAVENOUS",
"StartMarketingDate": "20180801",
"EndMarketingDate": "20251130",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090560",
"LabelerName": "Athenex Pharmaceutical Division, LLC.",
"SubstanceName": "NAFCILLIN SODIUM",
"StrengthNumber": "2",
"StrengthUnit": "g/1",
"Pharm_Classes": "Penicillin-class Antibacterial [EPC], Penicillins [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-12-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20180801",
"EndMarketingDatePackage": "20251130",
"SamplePackage": "N"
}
}