71610-964-31 : NDC 2026 Code

71610-964-31 : Naltrexone Hydrochloride ( Naltrexone Hydrochloride )

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NDC Code : 71610-964-31 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71610-964-31",
    "PackageDescription": "600 TABLET, FILM COATED in 1 BOTTLE (71610-964-31) ",
    "NDC11Code": "71610-0964-31",
    "ProductNDC": "71610-964",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Naltrexone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Naltrexone Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20020322",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076264",
    "LabelerName": "Aphena Pharma Solutions - Tennessee, LLC",
    "SubstanceName": "NALTREXONE HYDROCHLORIDE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Opioid Antagonist [EPC], Opioid Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-11-19",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251113",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}