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53746-082-30 : NDC 2026 Code

53746-082-30 : Lurasidone Hydrochloride ( Lurasidone Hydrochloride )

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NDC Code : 53746-082-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "53746-082-30",
    "PackageDescription": "30 TABLET, COATED in 1 BOTTLE (53746-082-30) ",
    "NDC11Code": "53746-0082-30",
    "ProductNDC": "53746-082",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lurasidone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lurasidone Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240705",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA208002",
    "LabelerName": "Amneal Pharmaceuticals of New York LLC",
    "SubstanceName": "LURASIDONE HYDROCHLORIDE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Atypical Antipsychotic [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-07-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240705",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}
                
            

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