EU active substance registration
Hikma Farmacêutica (Portugal), S.A.
EU active substance registration 002/SA/2018 · Portugal
Key facts
| Registration number | 002/SA/2018 |
|---|---|
| EudraGMDP reference | 12083 |
| Registration holder | Hikma Farmacêutica (Portugal), S.A. |
| Registered site | Hikma Farmacêutica (Portugal), S.A. |
| Site address | Estrada do Rio da Mó, n.º 8, 8-A e 8-B, Fervença, Sintra, 2705-906 Terrugem SNT |
| Country | Portugal |
| Competent authority | PT_INFARMED |
| National site reference | 002_SA/2018 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 10–99 Third-country API manufacturing sites
- Argentina, Brazil, China, India, Israel, JORDAN, Korea, Republic of, South Africa 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.