51991-892-33 : NDC 2026 Code

51991-892-33 : Erlotinib Hydrochloride ( Erlotinib )

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NDC Code : 51991-892-33 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51991-892-33",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (51991-892-33) ",
    "NDC11Code": "51991-0892-33",
    "ProductNDC": "51991-892",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Erlotinib",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Erlotinib Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20191105",
    "EndMarketingDate": "20250731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA208488",
    "LabelerName": "Breckenridge Pharmaceutical, Inc.",
    "SubstanceName": "ERLOTINIB HYDROCHLORIDE",
    "StrengthNumber": "150",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-08-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20191105",
    "EndMarketingDatePackage": "20250731",
    "SamplePackage": "N"
  }
}