{
"NDC": {
"NDCCode": "74074-003-99",
"PackageDescription": "1000 TABLET in 1 BOTTLE (74074-003-99) ",
"NDC11Code": "74074-0003-99",
"ProductNDC": "74074-003",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Meclizine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Meclizine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20201015",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA010721",
"LabelerName": "Nortic Pharma, LLC",
"SubstanceName": "MECLIZINE HYDROCHLORIDE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiemetic [EPC], Emesis Suppression [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-12-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20201015",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}