60687-889-83 : NDC 2026 Code

60687-889-83 : Budesonide ( Budesonide )

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NDC Code : 60687-889-83 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-889-83",
    "PackageDescription": "30 POUCH in 1 CARTON (60687-889-83)  / 1 AMPULE in 1 POUCH (60687-889-79)  / 2 mL in 1 AMPULE",
    "NDC11Code": "60687-0889-83",
    "ProductNDC": "60687-889",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Budesonide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Budesonide",
    "DosageFormName": "SUSPENSION",
    "RouteName": "RESPIRATORY (INHALATION)",
    "StartMarketingDate": "20260503",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211922",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "BUDESONIDE",
    "StrengthNumber": ".25",
    "StrengthUnit": "mg/2mL",
    "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-05-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260503",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}