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United States · US · US:22840-1350_36ac4a35-6d7b-a249-e063-6294a90a0b70
Prairie Mugwort Darkleaved Sagebrush
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11228401350210 mL in 1 VIAL, MULTI-DOSE (22840-1350-2)
- ndc11228401350450 mL in 1 VIAL, MULTI-DOSE (22840-1350-4)
Annotations
UNII (FDA Substance ID)
57KIJ4772H
ARTEMISIA LUDOVICIANA POLLEN
Raw payload (JSON)
{
"unii": {
"unii": "57KIJ4772H",
"rxcui": null,
"inchikey": null,
"display_name": "ARTEMISIA LUDOVICIANA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-1350_36ac4a35-6d7b-a249-e063-6294a90a0b70",
"productndc": "22840-1350",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "ARTEMISIA LUDOVICIANA POLLEN",
"proprietary_name": "Prairie Mugwort Darkleaved Sagebrush",
"active_ingred_unit": "[PNU]/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Artemisia ludoviciana",
"start_marketing_date": "19810915",
"active_numerator_strength": "20000"
}Access this data programmatically
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