50580-586-01 : NDC 2026 Code

50580-586-01 : Acetaminophen And Dextromethorphan Hydrobromide ( Extra Strength Tylenol Cold Plus Flu Multi Symptom Day )

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NDC Code : 50580-586-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50580-586-01",
    "PackageDescription": "2 BLISTER PACK in 1 CARTON (50580-586-01)  / 12 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "50580-0586-01",
    "ProductNDC": "50580-586",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Extra Strength Tylenol Cold Plus Flu Multi Symptom Day",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Acetaminophen And Dextromethorphan Hydrobromide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260618",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M012",
    "LabelerName": "Kenvue Brands LLC",
    "SubstanceName": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE",
    "StrengthNumber": "500; 15",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-06-24",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260618",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}