11822-7156-0 : NDC 2026 Code

11822-7156-0 : Guaifenesin And Dextromethorphan Hydrobromide ( Guaifenesin And Dextromethorphan Hydrobromide )

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NDC Code : 11822-7156-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "11822-7156-0",
    "PackageDescription": "1 BLISTER PACK in 1 CARTON (11822-7156-0)  &gt; 28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK",
    "NDC11Code": "11822-7156-00",
    "ProductNDC": "11822-7156",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Guaifenesin And Dextromethorphan Hydrobromide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Guaifenesin And Dextromethorphan Hydrobromide",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170905",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA021620",
    "LabelerName": "Rite-Aid",
    "SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
    "StrengthNumber": "60; 1200",
    "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": "Deprecated",
    "LastUpdate": "2023-01-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20170907",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}