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United States · US · US:22840-0201_37385fc6-1cdd-8aa6-e063-6294a90a6017
Standardized Kentucky (June) Bluegrass Pollen
UNIISPL
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
- ndc11228400201210 mL in 1 VIAL, MULTI-DOSE (22840-0201-2)
- ndc11228400201450 mL in 1 VIAL, MULTI-DOSE (22840-0201-4)
- ndc1122840020155 mL in 1 BOTTLE, DROPPER (22840-0201-5)
Annotations
UNII (FDA Substance ID)
SCB8J7LS3T
POA PRATENSIS POLLEN
RxCUI 852834
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SCB8J7LS3T",
"rxcui": "852834",
"inchikey": null,
"display_name": "POA PRATENSIS POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"3e65b958-03cd-4f8c-a6a0-990b53ae7ab4": {
"match": "brand_token",
"title": "STANDARDIZED CAT PELT INJECTION, SOLUTION [JUBILANT HOLLISTERSTIER LLC]",
"spl_version": "17",
"published_date": "2026-04-06"
}
},
"productid": "22840-0201_37385fc6-1cdd-8aa6-e063-6294a90a6017",
"productndc": "22840-0201",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "STANDARDIZED ALLERGENIC",
"substance_name": "POA PRATENSIS POLLEN",
"proprietary_name": "Standardized Kentucky (June) Bluegrass Pollen",
"active_ingred_unit": "[BAU]/mL",
"application_number": "BLA101837",
"marketing_category": "BLA",
"nonproprietary_name": "Poa pratensis",
"start_marketing_date": "19680915",
"active_numerator_strength": "10000"
}Access this data programmatically
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