Back to search

United States· US:65044-5048_b92e5087-bcde-4bcc-a899-2e078a039d30

Molds, Rusts and Smuts, Botrytis cinerea

A medicinal product containing botrytis cinerea, registered in United States by Jubilant HollisterStier LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMolds, Rusts and Smuts, Botrytis cine…ATC—REGISTER NO.US:65044-5048_b92e508…PACKS LISTED3CHECKEDJune 3, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
Botrytis cinerea
Manufacturer
Jubilant HollisterStier LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 3, 2026

Packs & prices · 3

  • ndc11
    6504450482
    10 mL in 1 VIAL (65044-5048-2)
  • ndc11
    6504450483
    30 mL in 1 VIAL (65044-5048-3)
  • ndc11
    6504450484
    50 mL in 1 VIAL (65044-5048-4)

Regulatory notes

UNII (FDA substance ID)
TBW53313S7
BOTRYTIS CINEREA
RxCUI 466195

Same medicine, other countries

Botrytis cinerea in 2 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All botrytis cinerea products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Germany · Prick-Testlösung Botrytis Cinerea, Provokations-Testlösung Botrytis Cinerea
  • Hungary · Alyostal Prick Penészgombák Allergén Kivonatot Tartalmazó Oldatok, Allergiás Betegségek Diagnosztizálásában Használatos Prick Tesztek Végzésére, Staloral

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/017c0e85-e820-4a49-928f-34f1dfaed9de
GET /v1/drugs/017c0e85-e820-4a49-928f-34f1dfaed9de?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "unii": {
    "unii": "TBW53313S7",
    "rxcui": "466195",
    "inchikey": null,
    "display_name": "BOTRYTIS CINEREA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "65044-5048_b92e5087-bcde-4bcc-a899-2e078a039d30",
  "productndc": "65044-5048",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BOTRYTIS CINEREA",
  "proprietary_name": "Molds, Rusts and Smuts, Botrytis cinerea",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA103888",
  "marketing_category": "BLA",
  "nonproprietary_name": "Botrytis cinerea",
  "start_marketing_date": "19410419",
  "active_numerator_strength": ".1"
}

See everything about botrytis cinerea.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.