58605-422-02 : NDC 2025 Code

58605-422-02 : Guaifenesin And Phenylephrine Hydrochloride ( Maxiphen )

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NDC Code : 58605-422-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "58605-422-02",
    "PackageDescription": "20 TABLET in 1 BLISTER PACK (58605-422-02)",
    "NDC11Code": "58605-0422-02",
    "ProductNDC": "58605-422",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Maxiphen",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Guaifenesin And Phenylephrine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20080331",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH FINAL",
    "ApplicationNumber": "part341",
    "LabelerName": "MCR American Pharmaceuticals, Inc.",
    "SubstanceName": "GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
    "StrengthNumber": "400; 10",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}