{
"NDC": {
"NDCCode": "61919-653-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (61919-653-30) ",
"NDC11Code": "61919-0653-30",
"ProductNDC": "61919-653",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Prochlorperazine Maleate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Prochlorperazine Maleate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20190419",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040185",
"LabelerName": "Direct_Rx",
"SubstanceName": "PROCHLORPERAZINE MALEATE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Phenothiazine [EPC], Phenothiazines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-11-22",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20190918",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}