72485-217-30 : NDC 2026 Code

72485-217-30 : Erlotinib Hydrochloride ( Erlotinib )

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NDC Code : 72485-217-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72485-217-30",
    "PackageDescription": "1 BOTTLE in 1 BOX (72485-217-30)  &gt; 30 TABLET, FILM COATED in 1 BOTTLE",
    "NDC11Code": "72485-0217-30",
    "ProductNDC": "72485-217",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Erlotinib",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Erlotinib Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20191106",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211960",
    "LabelerName": "Armas Pharmaceuticals Inc.",
    "SubstanceName": "ERLOTINIB HYDROCHLORIDE",
    "StrengthNumber": "25",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2019-11-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20191106",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}