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United States · US · US:37662-1305_e5fafb25-a010-65ba-e053-2a95a90a4228

Veratrum Album

UNIISPL

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

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
    3766213051
    200 PELLET in 1 VIAL, GLASS (37662-1305-1)
  • ndc11
    3766213052
    500 PELLET in 1 VIAL, GLASS (37662-1305-2)
  • ndc11
    3766213053
    3000 PELLET in 1 BOTTLE, GLASS (37662-1305-3)
  • ndc11
    3766213054
    10000 PELLET in 1 BOTTLE, GLASS (37662-1305-4)

Annotations

UNII (FDA Substance ID)
QNS6W5US1Z
VERATRUM ALBUM ROOT
RxCUI 285168
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "QNS6W5US1Z",
    "rxcui": "285168",
    "inchikey": null,
    "display_name": "VERATRUM ALBUM ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "63597f2a-22c1-41c2-b461-3517447cc03e": {
      "match": "brand_token",
      "title": "VERATRUM COMBINATION 9250 (VERATRUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1305_e5fafb25-a010-65ba-e053-2a95a90a4228",
  "productndc": "37662-1305",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "VERATRUM ALBUM ROOT",
  "proprietary_name": "Veratrum Album",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Veratrum Album",
  "start_marketing_date": "20220811",
  "active_numerator_strength": "200"
}

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