70518-3985-0 : NDC 2026 Code

70518-3985-0 : Lurasidone Hydrochloride ( Lurasidone Hydrochloride )

Additionally :

You can get information about “70518-3985-0” NDC code in 70518-3985-0 in HTML format

HTML | 70518-3985-0 in TXT (Plain Text) format

TXT | 70518-3985-0 in PDF (Portable Document Format)

PDF | 70518-3985-0 in XML format

XML formats.

NDC Code : 70518-3985-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-3985-0",
    "PackageDescription": "30 TABLET, COATED in 1 BLISTER PACK (70518-3985-0) ",
    "NDC11Code": "70518-3985-00",
    "ProductNDC": "70518-3985",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lurasidone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lurasidone Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240119",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA208002",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "LURASIDONE HYDROCHLORIDE",
    "StrengthNumber": "40",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Atypical Antipsychotic [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-08-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20240119",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}