70069-836-01 : NDC 2026 Code

70069-836-01 : Bortezomib ( Bortezomib )

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NDC Code : 70069-836-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70069-836-01",
    "PackageDescription": "1 VIAL in 1 CARTON (70069-836-01)  / 3.5 mL in 1 VIAL",
    "NDC11Code": "70069-0836-01",
    "ProductNDC": "70069-836",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bortezomib",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bortezomib",
    "DosageFormName": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
    "RouteName": "INTRAVENOUS; SUBCUTANEOUS",
    "StartMarketingDate": "20250429",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211898",
    "LabelerName": "Somerset Therapeutics LLC",
    "SubstanceName": "BORTEZOMIB",
    "StrengthNumber": "3.5",
    "StrengthUnit": "mg/3.5mL",
    "Pharm_Classes": "Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-05-12",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250429",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}