FDA — authorised 21 January 1987
- Application: NDA018963
- Marketing authorisation holder: BRACCO
- Local brand name: CHOLETEC
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Choletec on 21 January 1987
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 January 1987; FDA has authorised it.
BRACCO holds the US marketing authorisation.