EU active substance registration
Mundipharma DC B.V.
EU active substance registration 6871 API · Netherlands
Key facts
| Registration number | 6871 API |
|---|---|
| EudraGMDP reference | 14694 |
| Registration holder | Mundipharma DC B.V., LEUSDEN |
| Registered site | Mundipharma DC B.V. |
| Site address | Leusderend 16, LEUSDEN, 3832RC |
| Country | Netherlands |
| Competent authority | NL_FARMATEC |
| National site reference | FUSY/40314 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- Japan 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.