FDA — authorised 17 May 1983
- Marketing authorisation holder: SANDOZ
- Status: approved
🇺🇸 Actidil in United States
FDA authorised Actidil on 17 May 1983
Marketing authorisations
FDA
- Application: NDA011110
- Marketing authorisation holder: GLAXOSMITHKLINE
- Local brand name: ACTIDIL
- Indication: TABLET — ORAL
- Status: approved
Actidil in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Infectious Disease approved in United States
Frequently asked questions
Is Actidil approved in United States?
Yes. FDA authorised it on 17 May 1983; FDA has authorised it.
Who is the marketing authorisation holder for Actidil in United States?
SANDOZ holds the US marketing authorisation.