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United States · US · US:22840-5468_36ac4a35-6d79-a249-e063-6294a90a0b70
Lombardys Poplar 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
- ndc11228405468210 mL in 1 VIAL, MULTI-DOSE (22840-5468-2)
- ndc11228405468450 mL in 1 VIAL, MULTI-DOSE (22840-5468-4)
- ndc1122840546855 mL in 1 BOTTLE, DROPPER (22840-5468-5)
Annotations
UNII (FDA Substance ID)
0MGE63QPFJ
POPULUS NIGRA POLLEN
RxCUI 852348
Raw payload (JSON)
{
"unii": {
"unii": "0MGE63QPFJ",
"rxcui": "852348",
"inchikey": null,
"display_name": "POPULUS NIGRA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5468_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5468",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "POPULUS NIGRA POLLEN",
"proprietary_name": "Lombardys Poplar Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Populus nigra",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025"
}Access this data programmatically
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