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United States · US · US:22840-5444_36ac4a35-6d79-a249-e063-6294a90a0b70
Paper Mulberry 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
- ndc11228405444210 mL in 1 VIAL, MULTI-DOSE (22840-5444-2)
- ndc11228405444450 mL in 1 VIAL, MULTI-DOSE (22840-5444-4)
- ndc1122840544455 mL in 1 BOTTLE, DROPPER (22840-5444-5)
Annotations
UNII (FDA Substance ID)
51I6N3XIML
BROUSSONETIA PAPYRIFERA POLLEN
Raw payload (JSON)
{
"unii": {
"unii": "51I6N3XIML",
"rxcui": null,
"inchikey": null,
"display_name": "BROUSSONETIA PAPYRIFERA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5444_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5444",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "BROUSSONETIA PAPYRIFERA POLLEN",
"proprietary_name": "Paper Mulberry Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Broussonetia papyrifera",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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