62011-0376-1 : NDC 2026 Code

62011-0376-1 : Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride ( Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride )

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NDC Code : 62011-0376-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "62011-0376-1",
    "PackageDescription": "2 BLISTER PACK in 1 CARTON (62011-0376-1)  &gt; 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK",
    "NDC11Code": "62011-0376-01",
    "ProductNDC": "62011-0376",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20171030",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA209116",
    "LabelerName": "McKESSON Corporation",
    "SubstanceName": "FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE",
    "StrengthNumber": "60; 120",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-12-12",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20171030",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}