FDA — authorised 23 December 1991
- Application: NDA050664
- Marketing authorisation holder: CORDEN PHARMA
- Local brand name: CEFZIL
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Cefzil® on 23 December 1991
Yes. FDA authorised it on 23 December 1991; FDA authorised it on 23 December 1991.
CORDEN PHARMA holds the US marketing authorisation.