70154-112-08 : NDC 2026 Code

70154-112-08 : Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride ( Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride )

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NDC Code : 70154-112-08 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70154-112-08",
    "PackageDescription": "240 mL in 1 BOTTLE (70154-112-08) ",
    "NDC11Code": "70154-0112-08",
    "ProductNDC": "70154-112",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride",
    "DosageFormName": "LIQUID",
    "RouteName": "ORAL",
    "StartMarketingDate": "20190819",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH FINAL",
    "ApplicationNumber": "part341",
    "LabelerName": "Monarch PCM, LLC.",
    "SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
    "StrengthNumber": "18; 200; 10",
    "StrengthUnit": "mg/15mL; mg/15mL; mg/15mL",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-05-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20190819",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}