48951-2157-2 : NDC 2026 Code

48951-2157-2 : Berberis Larix ( Berberis Larix )

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NDC Code : 48951-2157-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "48951-2157-2",
    "PackageDescription": "1350 PELLET in 1 BOTTLE, GLASS (48951-2157-2) ",
    "NDC11Code": "48951-2157-02",
    "ProductNDC": "48951-2157",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Berberis Larix",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Berberis Larix",
    "DosageFormName": "PELLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20090901",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
    "ApplicationNumber": null,
    "LabelerName": "Uriel Pharmacy Inc",
    "SubstanceName": "ACHILLEA MILLEFOLIUM; APIS MELLIFERA; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; FERROUS DISULFIDE; LARIX DECIDUA RESIN; LYTTA VESICATORIA; SUS SCROFA URINARY BLADDER",
    "StrengthNumber": "3; 8; 3; 3; 8; 8; 6; 8",
    "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
    "Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20090901",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}