51672-2089-2 : NDC 2026 Code

51672-2089-2 : Diphenhydramine Hydrochloride And Zinc Acetate ( Diphenhydramine Hydrochloride And Zinc Acetate )

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NDC Code : 51672-2089-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51672-2089-2",
    "PackageDescription": "1 TUBE in 1 CARTON (51672-2089-2)  / 28.4 g in 1 TUBE",
    "NDC11Code": "51672-2089-02",
    "ProductNDC": "51672-2089",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Diphenhydramine Hydrochloride And Zinc Acetate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diphenhydramine Hydrochloride And Zinc Acetate",
    "DosageFormName": "CREAM",
    "RouteName": "TOPICAL",
    "StartMarketingDate": "20050920",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M017",
    "LabelerName": "Sun Pharmaceutical Industries, Inc.",
    "SubstanceName": "DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE",
    "StrengthNumber": "20; 1",
    "StrengthUnit": "mg/g; mg/g",
    "Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-07-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20050920",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}