FDA — authorised 24 September 1996
- Application: NDA020533
- Marketing authorisation holder: FRESENIUS KABI USA
- Local brand name: NAROPIN
- Indication: SOLUTION — INJECTION
- Status: approved
FDA authorised Naropin on 24 September 1996
Yes. FDA authorised it on 24 September 1996.
FRESENIUS KABI USA holds the US marketing authorisation.