60687-421-25 : NDC 2026 Code

60687-421-25 : Budesonide ( Budesonide )

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NDC Code : 60687-421-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-421-25",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-421-25)  &gt; 1 CAPSULE in 1 BLISTER PACK (60687-421-95) ",
    "NDC11Code": "60687-0421-25",
    "ProductNDC": "60687-421",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Budesonide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Budesonide",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20181218",
    "EndMarketingDate": "20200531",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA207367",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "BUDESONIDE",
    "StrengthNumber": "3",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-06-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20181218",
    "EndMarketingDatePackage": "20200531",
    "SamplePackage": "N"
  }
}