EU active substance registration
HIKMA ITALIA S.P.A.
EU active substance registration API - 108/2021 · Italy
Key facts
| Registration number | API - 108/2021 |
|---|---|
| EudraGMDP reference | 32565 |
| Registration holder | HIKMA ITALIA S.P.A. |
| Registered site | HIKMA ITALIA S.P.A. |
| Site address | VIALE CERTOSA, 10, PAVIA, 27100 |
| Country | Italy |
| Competent authority | IT_AIFA |
| National site reference | 100221 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- China Supplier countries outside the EEA
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About EU active substance (API) registrations
Companies in the EEA that manufacture, import or distribute active substances for human medicines must register with their national competent authority. EudraGMDP publishes each registration and the third-country sites that supply the substances.