FDA — authorised 21 October 1988
- Application: NDA019667
- Marketing authorisation holder: NOVARTIS
- Local brand name: SANDOSTATIN
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised SOM230 LAR on 21 October 1988
Yes. FDA authorised it on 21 October 1988.
NOVARTIS holds the US marketing authorisation.