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United States · US · US:0268-1417_028ad0ff-1a2d-4610-bf84-a0eaacaf599e
MIXED RAGWEED
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerALK-Abello, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11026814171010 mL in 1 VIAL (0268-1417-10)
- ndc11026814175050 mL in 1 VIAL (0268-1417-50)
Annotations
UNII (FDA Substance ID)
K20Y81ACO3
AMBROSIA ARTEMISIIFOLIA POLLEN
RxCUI 896135
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "K20Y81ACO3",
"rxcui": "896135",
"inchikey": null,
"display_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"304ff4db-201a-60a4-e054-00144ff8d46c": {
"match": "brand_token",
"title": "MIXED BERRY SORE THROAT AND COUGH LOZENGE (DEXTROMETHORPHAN HYDROBROMIDE) LOZENGE [MEIJER DISTRIBUTION, INC.]",
"spl_version": "8",
"published_date": "2026-02-03"
}
},
"productid": "0268-1417_028ad0ff-1a2d-4610-bf84-a0eaacaf599e",
"productndc": "0268-1417",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN",
"proprietary_name": "MIXED RAGWEED",
"active_ingred_unit": "g/mL; g/mL",
"application_number": "BLA103753",
"marketing_category": "BLA",
"nonproprietary_name": "MIXED RAGWEED",
"start_marketing_date": "20150503",
"active_numerator_strength": ".1; .1"
}Access this data programmatically
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