41163-510-02 : NDC 2026 Code

41163-510-02 : Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride ( Daytime Severe Cold And Flu Relief )

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NDC Code : 41163-510-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "41163-510-02",
    "PackageDescription": "1 BLISTER PACK in 1 CARTON (41163-510-02)  &gt; 12 TABLET, COATED in 1 BLISTER PACK",
    "NDC11Code": "41163-0510-02",
    "ProductNDC": "41163-510",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Daytime Severe Cold And Flu Relief",
    "ProprietaryNameSuffix": "Maximum Strength",
    "NonProprietaryName": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20140801",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH FINAL",
    "ApplicationNumber": "part341",
    "LabelerName": "Supervalu Inc.",
    "SubstanceName": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
    "StrengthNumber": "325; 10; 200; 5",
    "StrengthUnit": "mg/1; mg/1; mg/1; mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-10-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20140801",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}