FDA — authorised 22 May 2018
- Application: NDA210308
- Marketing authorisation holder: SUN PHARM
- Local brand name: YONSA
- Indication: TABLET — ORAL
- Status: approved
FDA authorised abiraterone acetate with Methylprednisolone on 22 May 2018
Yes. FDA authorised it on 22 May 2018.
SUN PHARM holds the US marketing authorisation.