FDA — authorised 23 October 1946
- Marketing authorisation holder: NOVARTIS
- Status: approved
🇺🇸 Mesantoin in United States
FDA authorised Mesantoin on 23 October 1946
Marketing authorisations
FDA — authorised 23 October 1946
- Application: NDA006008
- Marketing authorisation holder: NOVARTIS
- Local brand name: MESANTOIN
- Indication: TABLET — ORAL
- Status: approved
Mesantoin in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Neuroscience approved in United States
Frequently asked questions
Is Mesantoin approved in United States?
Yes. FDA authorised it on 23 October 1946; FDA authorised it on 23 October 1946.
Who is the marketing authorisation holder for Mesantoin in United States?
NOVARTIS holds the US marketing authorisation.