FDA — authorised 28 February 2018
- Application: NDA207962
- Marketing authorisation holder: SCILEX PHARMS
- Local brand name: ZTLIDO
- Indication: PATCH — TOPICAL
- Status: approved
FDA authorised ZTlido on 28 February 2018
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 28 February 2018; FDA has authorised it.
SCILEX PHARMS holds the US marketing authorisation.