# BOTOX

NDC: 85766-155
Generic name: onabotulinumtoxinA
Labeler / Manufacturer: Sportpharm LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRADERMAL, INTRAMUSCULAR
Marketing started: 19891215

FDA application: BLA103000

## 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:"85766-155"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85766-155
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6f42753-d31e-4b23-8da0-4b990fee4b38