# Dysport

NDC: 0299-5962
Generic name: Botulinum Toxin Type A
Labeler / Manufacturer: Galderma Laboratories, L.P.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20091102

FDA application: BLA125274

## Active ingredients

- BOTULINUM TOXIN TYPE A: 300 U/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0299-5962"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0299-5962
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=71313a04-1349-4c26-b840-a39e4a3ddaed