Fusarium moniliforme

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
2284016722
10 mL in 1 VIAL, MULTI-DOSE (22840-1672-2)

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": "22840-1672_36ac182a-ff48-50a9-e063-6394a90aa917",
  "productndc": "22840-1672",
  "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"
}

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