FDA — authorised 6 August 2020
- Application: NDA213464
- Marketing authorisation holder: BAYER HEALTHCARE
- Local brand name: LAMPIT
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Lampit on 6 August 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 6 August 2020.
BAYER HEALTHCARE holds the US marketing authorisation.