FDA — authorised 24 July 2020
- Application: NDA206966
- Marketing authorisation holder: LNHC
- Local brand name: XEGLYZE
- Indication: LOTION — TOPICAL
- Status: approved
FDA authorised Xeglyze on 24 July 2020
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 24 July 2020; FDA has authorised it.
LNHC holds the US marketing authorisation.