# Jeuveau

NDC: 72301-595
Generic name: Prabotulinum Toxin Type A
Labeler / Manufacturer: Evolus, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: POWDER
Routes: INTRAMUSCULAR
Marketing started: 20190213

FDA application: BLA761085

## Active ingredients

- BOTULINUM TOXIN TYPE A: 100 [USP'U]/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72301-595"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72301-595
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=17a914c1-e54b-4b50-965d-b0fd9111bba4