Botrytis

UNII

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

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964310405
5 mL in 1 VIAL, MULTI-DOSE (49643-104-05)
ndc11
4964310410
10 mL in 1 VIAL, MULTI-DOSE (49643-104-10)
ndc11
4964310430
30 mL in 1 VIAL, MULTI-DOSE (49643-104-30)
ndc11
4964310450
50 mL in 1 VIAL, MULTI-DOSE (49643-104-50)

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": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-104_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-104",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BOTRYTIS CINEREA",
  "proprietary_name": "Botrytis",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Botrytis cinerea",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".1"
}

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