# Xeomin

NDC: 0259-4150
Generic name: incobotulinumtoxinA
Labeler / Manufacturer: Merz Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20100901

FDA application: BLA125360

## Active ingredients

- BOTULINUM TOXIN TYPE A: 50 [USP'U]/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0259-4150"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0259-4150
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ccdc3aae-6e2d-4cd0-a51c-8375bfee9458