48951-8318-2 : NDC 2026 Code

48951-8318-2 : Purple Coneflower ( Purple Coneflower )

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NDC Code : 48951-8318-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "48951-8318-2",
    "PackageDescription": "360 SPRAY in 1 BOTTLE, SPRAY (48951-8318-2)",
    "NDC11Code": "48951-8318-02",
    "ProductNDC": "48951-8318",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Purple Coneflower",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Purple Coneflower",
    "DosageFormName": "SPRAY",
    "RouteName": "ORAL",
    "StartMarketingDate": "20090901",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
    "ApplicationNumber": null,
    "LabelerName": "Uriel Pharmacy Inc",
    "SubstanceName": "ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA PALLIDA; EUCALYPTUS GLOBULUS LEAF; MERCURIC CYANIDE; SAGE; SILICON DIOXIDE; SILVER NITRATE",
    "StrengthNumber": "20; 1; 1; 1; 8; 1; 20; 20",
    "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], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}