Viburnum Opulus

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766213461
200 PELLET in 1 VIAL, GLASS (37662-1346-1)
ndc11
3766213462
500 PELLET in 1 VIAL, GLASS (37662-1346-2)
ndc11
3766213463
3000 PELLET in 1 BOTTLE, GLASS (37662-1346-3)
ndc11
3766213464
10000 PELLET in 1 BOTTLE, GLASS (37662-1346-4)

Annotations

UNII (FDA Substance ID)

T1UG6H6805

VIBURNUM OPULUS BARK

RxCUI 1809840

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "T1UG6H6805",
    "rxcui": "1809840",
    "inchikey": null,
    "display_name": "VIBURNUM OPULUS BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a73d299-23a2-a3bf-e063-6394a90a6fea": {
      "match": "brand_token",
      "title": "VIBURNUM OPULUS (VIBURNUM OPULUS BARK) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-20"
    }
  },
  "productid": "37662-1346_e6115854-4d17-730a-e053-2a95a90a125a",
  "productndc": "37662-1346",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "VIBURNUM OPULUS BARK",
  "proprietary_name": "Viburnum Opulus",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Viburnum Opulus",
  "start_marketing_date": "20220812",
  "active_numerator_strength": "500"
}

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