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United States · US · US:0220-0219_10e04d03-329d-090f-e063-6294a90a6c72
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 · 2
- ndc11022002194130 [hp_C] in 1 TUBE (0220-0219-41)
- ndc1102200219433 TUBE in 1 PACKAGE (0220-0219-43) / 30 [hp_C] in 1 TUBE
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": "0220-0219_10e04d03-329d-090f-e063-6294a90a6c72",
"productndc": "0220-0219",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AMBROSIA ARTEMISIIFOLIA",
"proprietary_name": "Ambrosia artemisiaefolia",
"active_ingred_unit": "[hp_C]/30[hp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "AMBROSIA ARTEMISIIFOLIA",
"start_marketing_date": "19830303",
"active_numerator_strength": "30"
}Access this data programmatically
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