FDA — authorised 21 July 2023
- Application: NDA212905
- Marketing authorisation holder: VERRICA PHARMS
- Local brand name: YCANTH
- Indication: SOLUTION — TOPICAL
- Status: approved
FDA authorised Ycanth on 21 July 2023
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 July 2023.
VERRICA PHARMS holds the US marketing authorisation.