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United States · US · US:37662-2165_f04c4aae-b795-1d15-e053-2a95a90a993f
Stramonium
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 · 3
- ndc113766221651200 PELLET in 1 VIAL, GLASS (37662-2165-1)
- ndc1137662216521200 PELLET in 1 BOTTLE, GLASS (37662-2165-2)
- ndc1137662216534000 PELLET in 1 BOTTLE, GLASS (37662-2165-3)
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": "37662-2165_f04c4aae-b795-1d15-e053-2a95a90a993f",
"productndc": "37662-2165",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DATURA STRAMONIUM",
"proprietary_name": "Stramonium",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Stramonium",
"start_marketing_date": "20221220",
"active_numerator_strength": "6"
}Access this data programmatically
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