{
"NDC": {
"NDCCode": "70518-1936-0",
"PackageDescription": "30 POUCH in 1 BOX, UNIT-DOSE (70518-1936-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-1936-1) ",
"NDC11Code": "70518-1936-00",
"ProductNDC": "70518-1936",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Latuda",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lurasidone Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20190306",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA200603",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "LURASIDONE HYDROCHLORIDE",
"StrengthNumber": "120",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Atypical Antipsychotic [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-01-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20190306",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}