48433-221-40 : NDC 2026 Code

48433-221-40 : Guaifenesin And Dextromethorphan Hydrobromide ( Guaifenesin And Dextromethorphan Hbr )

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NDC Code : 48433-221-40 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "48433-221-40",
    "PackageDescription": "40 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (48433-221-40)  / 5 mL in 1 CUP, UNIT-DOSE (48433-221-05) ",
    "NDC11Code": "48433-0221-40",
    "ProductNDC": "48433-221",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Guaifenesin And Dextromethorphan Hbr",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Guaifenesin And Dextromethorphan Hydrobromide",
    "DosageFormName": "LIQUID",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220201",
    "EndMarketingDate": "20231001",
    "MarketingCategoryName": "OTC MONOGRAPH FINAL",
    "ApplicationNumber": "part341",
    "LabelerName": "Safecor Health, LLC",
    "SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
    "StrengthNumber": "10; 100",
    "StrengthUnit": "mg/5mL; mg/5mL",
    "Pharm_Classes": "Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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": "2023-10-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20220201",
    "EndMarketingDatePackage": "20231001",
    "SamplePackage": "N"
  }
}