FDA — authorised 27 April 1954
- Application: NDA009321
- Marketing authorisation holder: BRACCO
- Local brand name: CHOLOGRAFIN SODIUM
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Cholografin Meglumine on 27 April 1954
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 27 April 1954; FDA has authorised it.
BRACCO holds the US marketing authorisation.