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United States · US · US:22840-5607_36ac182a-ff48-50a9-e063-6394a90aa917
Aureobasidium pullulans
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
- ndc11228405607210 mL in 1 VIAL, MULTI-DOSE (22840-5607-2)
- ndc11228405607450 mL in 1 VIAL, MULTI-DOSE (22840-5607-4)
- ndc1122840560755 mL in 1 BOTTLE, DROPPER (22840-5607-5)
Annotations
UNII (FDA Substance ID)
D1A2NG69CK
AUREOBASIDIUM PULLULANS VAR. PULLUTANS
RxCUI 852102
Raw payload (JSON)
{
"unii": {
"unii": "D1A2NG69CK",
"rxcui": "852102",
"inchikey": null,
"display_name": "AUREOBASIDIUM PULLULANS VAR. PULLUTANS",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5607_36ac182a-ff48-50a9-e063-6394a90aa917",
"productndc": "22840-5607",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AUREOBASIDIUM PULLULANS VAR. PULLUTANS",
"proprietary_name": "Aureobasidium pullulans",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Aureobasidium pullulans",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025"
}Access this data programmatically
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