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United States · US · US:22840-5479_36ac4a35-6d79-a249-e063-6294a90a0b70
Siberian Elm Pollen
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 · 3
- ndc11228405479210 mL in 1 VIAL, MULTI-DOSE (22840-5479-2)
- ndc11228405479450 mL in 1 VIAL, MULTI-DOSE (22840-5479-4)
- ndc1122840547955 mL in 1 BOTTLE, DROPPER (22840-5479-5)
Annotations
UNII (FDA Substance ID)
030R993R8E
ULMUS PUMILA POLLEN
RxCUI 852844
Raw payload (JSON)
{
"unii": {
"unii": "030R993R8E",
"rxcui": "852844",
"inchikey": null,
"display_name": "ULMUS PUMILA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5479_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5479",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "ULMUS PUMILA POLLEN",
"proprietary_name": "Siberian Elm Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Ulmus pumila",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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