FDA — authorised 27 April 1955
- Application: NDA009866
- Marketing authorisation holder: PHARMACIA AND UPJOHN
- Status: supplemented
🇺🇸 Solu-Cortef in United States
FDA authorised Solu-Cortef on 27 April 1955
Marketing authorisation
Frequently asked questions
Is Solu-Cortef approved in United States?
Yes. FDA authorised it on 27 April 1955.
Who is the marketing authorisation holder for Solu-Cortef in United States?
PHARMACIA AND UPJOHN holds the US marketing authorisation.