70954-909-10 : NDC 2026 Code

70954-909-10 : Lofexidine ( Lofexidine )

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NDC Code : 70954-909-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70954-909-10",
    "PackageDescription": "36 TABLET in 1 BOTTLE (70954-909-10) ",
    "NDC11Code": "70954-0909-10",
    "ProductNDC": "70954-909",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lofexidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lofexidine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20251022",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA219917",
    "LabelerName": "ANI Pharmaceuticals, Inc.",
    "SubstanceName": "LOFEXIDINE HYDROCHLORIDE",
    "StrengthNumber": ".18",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-10-27",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251022",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}