FDA — authorised 19 December 2014
- Application: NDA206255
- Marketing authorisation holder: GALDERMA LABS LP
- Local brand name: SOOLANTRA
- Indication: CREAM — TOPICAL
- Status: approved
FDA authorised Ivermectin 1% cream on 19 December 2014
Yes. FDA authorised it on 19 December 2014.
GALDERMA LABS LP holds the US marketing authorisation.