{
"NDC": {
"NDCCode": "83008-022-30",
"PackageDescription": "30 TABLET in 1 BOTTLE (83008-022-30) ",
"NDC11Code": "83008-0022-30",
"ProductNDC": "83008-022",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Meclizine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Meclizine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20230505",
"EndMarketingDate": "20241031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA084657",
"LabelerName": "Quality Care Products, LLC",
"SubstanceName": "MECLIZINE HYDROCHLORIDE",
"StrengthNumber": "12.5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiemetic [EPC], Emesis Suppression [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-07-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20230505",
"EndMarketingDatePackage": "20240630",
"SamplePackage": "N"
}
}