Stramonium

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
3766221711
200 PELLET in 1 VIAL, GLASS (37662-2171-1)
ndc11
3766221712
500 PELLET in 1 VIAL, GLASS (37662-2171-2)
ndc11
3766221713
3000 PELLET in 1 BOTTLE, GLASS (37662-2171-3)
ndc11
3766221714
10000 PELLET in 1 BOTTLE, GLASS (37662-2171-4)

Annotations

UNII (FDA Substance ID)

G6W4F0V8Z3

DATURA STRAMONIUM

RxCUI 1310350

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G6W4F0V8Z3",
    "rxcui": "1310350",
    "inchikey": null,
    "display_name": "DATURA STRAMONIUM",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "34017893-a1d0-41d0-e063-6294a90a2b6a": {
      "match": "brand_token",
      "title": "STRAMONIUM 30X (DATURA STRAMONIUM 30X) LIQUID [TRUE BOTANICA, LLC]",
      "spl_version": "1",
      "published_date": "2025-06-13"
    }
  },
  "productid": "37662-2171_f04c4aae-b795-1d15-e053-2a95a90a993f",
  "productndc": "37662-2171",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DATURA STRAMONIUM",
  "proprietary_name": "Stramonium",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Stramonium",
  "start_marketing_date": "20221220",
  "active_numerator_strength": "1"
}

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