37835-165-50 : NDC 2026 Code

37835-165-50 : Famotidine ( Famotidine )

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NDC Code : 37835-165-50 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "37835-165-50",
    "PackageDescription": "50 TABLET in 1 BOTTLE (37835-165-50) ",
    "NDC11Code": "37835-0165-50",
    "ProductNDC": "37835-165",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Famotidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Famotidine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250601",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA215822",
    "LabelerName": "Bi-Mart",
    "SubstanceName": "FAMOTIDINE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-06-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250601",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}