FDA — authorised 24 September 1954
- Application: NDA009495
- Marketing authorisation holder: GLAXOSMITHKLINE
- Local brand name: MAREZINE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Marezine on 24 September 1954
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 September 1954; FDA has authorised it.
GLAXOSMITHKLINE holds the US marketing authorisation.