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United States · US · US:37662-1981_ee05578e-ca07-55c2-e053-2995a90af56f

Nux Vomica

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
    3766219811
    200 PELLET in 1 VIAL, GLASS (37662-1981-1)
  • ndc11
    3766219812
    500 PELLET in 1 VIAL, GLASS (37662-1981-2)
  • ndc11
    3766219813
    3000 PELLET in 1 BOTTLE, GLASS (37662-1981-3)
  • ndc11
    3766219814
    10000 PELLET in 1 BOTTLE, GLASS (37662-1981-4)

Annotations

UNII (FDA Substance ID)
269XH13919
STRYCHNOS NUX-VOMICA SEED
RxCUI 1309678
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "269XH13919",
    "rxcui": "1309678",
    "inchikey": null,
    "display_name": "STRYCHNOS NUX-VOMICA SEED",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "28f6663d-0a00-4650-a84e-b625024687d3": {
      "match": "brand_token",
      "title": "NUX VOMICA COMBINATION 9235 (NUX VOMICA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1981_ee05578e-ca07-55c2-e053-2995a90af56f",
  "productndc": "37662-1981",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STRYCHNOS NUX-VOMICA SEED",
  "proprietary_name": "Nux Vomica",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Nux Vomica",
  "start_marketing_date": "20221121",
  "active_numerator_strength": "200"
}

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