72205-246-42 : NDC 2026 Code

72205-246-42 : Lofexidine Hydrochloride ( Lofexidine Hydrochloride )

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NDC Code : 72205-246-42 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72205-246-42",
    "PackageDescription": "1 BOTTLE in 1 CARTON (72205-246-42)  / 36 TABLET, FILM COATED in 1 BOTTLE",
    "NDC11Code": "72205-0246-42",
    "ProductNDC": "72205-246",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lofexidine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lofexidine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250224",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA218699",
    "LabelerName": "Novadoz Pharmaceuticals LLC",
    "SubstanceName": "LOFEXIDINE HYDROCHLORIDE",
    "StrengthNumber": ".2",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-03-10",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250301",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}