FDA — authorised 30 July 2010
- Application: BLA125360
- Marketing authorisation holder: MERZ PHARMS
- Local brand name: Xeomin
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Xeomin on 30 July 2010
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 30 July 2010; FDA has authorised it.
MERZ PHARMS holds the US marketing authorisation.