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United States · US · US:49643-336_36ad1e17-751d-e226-e063-6394a90ab328
Hackberry Pollen
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1149643336055 mL in 1 VIAL, MULTI-DOSE (49643-336-05)
- ndc11496433361010 mL in 1 VIAL, MULTI-DOSE (49643-336-10)
- ndc11496433363030 mL in 1 VIAL, MULTI-DOSE (49643-336-30)
- ndc11496433365050 mL in 1 VIAL, MULTI-DOSE (49643-336-50)
Annotations
UNII (FDA Substance ID)
68R9X9Y96X
CELTIS OCCIDENTALIS POLLEN
RxCUI 852324
Raw payload (JSON)
{
"unii": {
"unii": "68R9X9Y96X",
"rxcui": "852324",
"inchikey": null,
"display_name": "CELTIS OCCIDENTALIS POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
"productid": "49643-336_36ad1e17-751d-e226-e063-6394a90ab328",
"productndc": "49643-336",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "CELTIS OCCIDENTALIS POLLEN",
"proprietary_name": "Hackberry Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA102211",
"marketing_category": "BLA",
"nonproprietary_name": "Celtis occidentalis",
"start_marketing_date": "19740312",
"active_numerator_strength": ".05"
}Access this data programmatically
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