Phoma betae

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
2284026181
5 mL in 1 VIAL, MULTI-DOSE (22840-2618-1)

Annotations

UNII (FDA Substance ID)

V58BK047ES

PLEOSPORA BETAE

Raw payload (JSON)

{
  "unii": {
    "unii": "V58BK047ES",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PLEOSPORA BETAE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-2618_36ac182a-ff48-50a9-e063-6394a90aa917",
  "productndc": "22840-2618",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "PLEOSPORA BETAE",
  "proprietary_name": "Phoma betae",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Phoma betae",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".001"
}

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