{
"NDC": {
"NDCCode": "43063-607-10",
"PackageDescription": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-607-10)",
"NDC11Code": "43063-0607-10",
"ProductNDC": "43063-607",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Prochlorperazine Maleate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Prochlorperazine Maleate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "19961118",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040185",
"LabelerName": "PD-Rx Pharmaceuticals, Inc.",
"SubstanceName": "PROCHLORPERAZINE MALEATE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Phenothiazine [EPC],Phenothiazines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-25",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}