FDA — authorised 7 February 2007
- Application: NDA021887
- Marketing authorisation holder: HALEON US HOLDINGS
- Local brand name: ALLI
- Indication: CAPSULE — ORAL
- Status: approved
FDA authorised Combination of treatments on 7 February 2007
Yes. FDA authorised it on 7 February 2007.
HALEON US HOLDINGS holds the US marketing authorisation.