{
"NDC": {
"NDCCode": "51407-832-05",
"PackageDescription": "500 TABLET, FILM COATED in 1 BOTTLE (51407-832-05) ",
"NDC11Code": "51407-0832-05",
"ProductNDC": "51407-832",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lurasidone Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lurasidone Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20190904",
"EndMarketingDate": "20260930",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA208058",
"LabelerName": "Golden State Medical Supply, Inc.",
"SubstanceName": "LURASIDONE HYDROCHLORIDE",
"StrengthNumber": "40",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Atypical Antipsychotic [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-12-23",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20231023",
"EndMarketingDatePackage": "20260930",
"SamplePackage": "N"
}
}