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United States · US · US:37662-1979_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
- ndc11376621979180 PELLET in 1 VIAL, GLASS (37662-1979-1)
- ndc113766219792200 PELLET in 1 VIAL, GLASS (37662-1979-2)
- ndc1137662197931200 PELLET in 1 BOTTLE, GLASS (37662-1979-3)
- ndc1137662197944000 PELLET in 1 BOTTLE, GLASS (37662-1979-4)
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": "37662-1979_ee05578e-ca07-55c2-e053-2995a90af56f",
"productndc": "37662-1979",
"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": "30"
}Access this data programmatically
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