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United States · US · US:0220-2450_003a848f-c8d0-0cb1-e063-6294a90a6602

Helleborus niger

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBoiron
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0220245041
    200 [kp_C] in 1 TUBE (0220-2450-41)

Annotations

UNII (FDA Substance ID)
608DGJ6815
HELLEBORUS NIGER ROOT
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "608DGJ6815",
    "rxcui": null,
    "inchikey": null,
    "display_name": "HELLEBORUS NIGER ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "150e57ad-3ed7-5cc9-e063-6394a90a25fe": {
      "match": "brand_token",
      "title": "HELLEBORUS COMP. A LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "3",
      "published_date": "2025-11-24"
    }
  },
  "productid": "0220-2450_003a848f-c8d0-0cb1-e063-6294a90a6602",
  "productndc": "0220-2450",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HELLEBORUS NIGER ROOT",
  "proprietary_name": "Helleborus niger",
  "active_ingred_unit": "[kp_C]/200[kp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "HELLEBORUS NIGER ROOT",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "200"
}

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