BOTRYTIS CINEREA

UNII

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

Identification

ManufacturerALK-Abello, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0268809010
10.5 mL in 1 VIAL (0268-8090-10)
ndc11
0268809050
53 mL in 1 VIAL (0268-8090-50)

Annotations

UNII (FDA Substance ID)

TBW53313S7

BOTRYTIS CINEREA

RxCUI 466195

Raw payload (JSON)

{
  "unii": {
    "unii": "TBW53313S7",
    "rxcui": "466195",
    "inchikey": null,
    "display_name": "BOTRYTIS CINEREA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "productid": "0268-8090_85c04c83-76ad-4116-aeb7-bbb5a9ab23f3",
  "productndc": "0268-8090",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BOTRYTIS CINEREA",
  "proprietary_name": "BOTRYTIS CINEREA",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "BOTRYTIS CINEREA",
  "start_marketing_date": "19650101",
  "active_numerator_strength": ".1"
}

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