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United States · US · US:22840-5618_36ac182a-ff48-50a9-e063-6394a90aa917
Fusarium moniliforme
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
- ndc11228405618210 mL in 1 VIAL, MULTI-DOSE (22840-5618-2)
- ndc11228405618450 mL in 1 VIAL, MULTI-DOSE (22840-5618-4)
- ndc1122840561855 mL in 1 BOTTLE, DROPPER (22840-5618-5)
Annotations
UNII (FDA Substance ID)
815V716OR2
GIBBERELLA FUJIKUROI
Raw payload (JSON)
{
"unii": {
"unii": "815V716OR2",
"rxcui": null,
"inchikey": null,
"display_name": "GIBBERELLA FUJIKUROI",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5618_36ac182a-ff48-50a9-e063-6394a90aa917",
"productndc": "22840-5618",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "GIBBERELLA FUJIKUROI",
"proprietary_name": "Fusarium moniliforme",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Fusarium moniliforme",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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