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United States · US · US:37662-3654_01e66d3c-0a9b-0871-e063-6394a90ae891
Anacardium Occidentale
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
- ndc113766236541200 PELLET in 1 VIAL, GLASS (37662-3654-1)
- ndc113766236542500 PELLET in 1 VIAL, GLASS (37662-3654-2)
- ndc1137662365433000 PELLET in 1 BOTTLE, GLASS (37662-3654-3)
- ndc11376623654410000 PELLET in 1 BOTTLE, GLASS (37662-3654-4)
Annotations
UNII (FDA Substance ID)
4A10JR4E7E
ANACARDIUM OCCIDENTALE FRUIT
RxCUI 1358956
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4A10JR4E7E",
"rxcui": "1358956",
"inchikey": null,
"display_name": "ANACARDIUM OCCIDENTALE FRUIT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"98b62390-c29a-422e-98f9-ae1899fdcab6": {
"match": "brand_token",
"title": "ANACARDIUM COMBINATION 9205 (ANACARDIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "37662-3654_01e66d3c-0a9b-0871-e063-6394a90ae891",
"productndc": "37662-3654",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ANACARDIUM OCCIDENTALE FRUIT",
"proprietary_name": "Anacardium Occidentale",
"active_ingred_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Anacardium Occidentale",
"start_marketing_date": "20230801",
"active_numerator_strength": "1"
}Access this data programmatically
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