Botrytis cinerea

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 · 3

ndc11
2284056092
10 mL in 1 VIAL, MULTI-DOSE (22840-5609-2)
ndc11
2284056094
50 mL in 1 VIAL, MULTI-DOSE (22840-5609-4)
ndc11
2284056095
5 mL in 1 BOTTLE, DROPPER (22840-5609-5)

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": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-5609_36ac182a-ff48-50a9-e063-6394a90aa917",
  "productndc": "22840-5609",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BOTRYTIS CINEREA",
  "proprietary_name": "Botrytis cinerea",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Botrytis cinerea",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".025"
}

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