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United States · US · US:0220-0230_0c069179-fc7d-cf6b-e063-6394a90aeaeb
AMBROSIA ARTEMISIAEFOLIA
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110220023041200 [kp_C] in 1 TUBE (0220-0230-41)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "ORAL",
"spl_meta": {
"8427717f-4d1a-54b5-e053-2a91aa0a3d00": {
"match": "brand_token",
"title": "AMBROSIA ARTEMISIAEFOLIA (AMBROSIA ARTEMISIIFOLIA\t) PELLET [BOIRON]",
"spl_version": "8",
"published_date": "2024-02-09"
}
},
"productid": "0220-0230_0c069179-fc7d-cf6b-e063-6394a90aeaeb",
"productndc": "0220-0230",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AMBROSIA ARTEMISIIFOLIA",
"proprietary_name": "AMBROSIA ARTEMISIAEFOLIA",
"active_ingred_unit": "[kp_C]/200[kp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "AMBROSIA ARTEMISIIFOLIA",
"start_marketing_date": "20240101",
"active_numerator_strength": "200"
}Access this data programmatically
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