# Botrytis

NDC: 49643-104
Generic name: Botrytis cinerea
Labeler / Manufacturer: Allermed Laboratories, Inc.
Product type: NON-STANDARDIZED ALLERGENIC
Marketing category: Biologic License Application
Dosage form: INJECTION
Routes: CUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Marketing started: 19740312

FDA application: BLA102211

## Active ingredients

- BOTRYTIS CINEREA: .1 g/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49643-104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49643-104