EU active substance registration
Sanofi-Aventis Deutschland GmbH
EU active substance registration DE_HE_01_REG_2020_1541 · Germany
Key facts
| Registration number | DE_HE_01_REG_2020_1541 |
|---|---|
| EudraGMDP reference | 23305 |
| Registration holder | Sanofi-Aventis Deutschland GmbH |
| Registered site | Sanofi-Aventis Deutschland GmbH |
| Site address | Brueningstrasse 50, Frankfurt am Main, Hessen, 65926 |
| Country | Germany |
| Competent authority | DE_HE_01 |
| National site reference | 00013720 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- None Third-country API manufacturing sites
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.