Register entry
Sachtleben Chemie International GmbH
Data as of · How to read this entry
- Registered sites
- 1
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 1
- Base
- Germany
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Labelling1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Sachtleben Chemiepark GmbHRegistrant: Sachtleben Chemie International GmbH | Dr.-Rudolf-Sachtleben-Str. 4, Duisburg, Nordrhein-Westfalen 47198, Germany (DEU) | Analytical testing, Active ingredient (API) manufacture, Labelling, Packaging | 1000180094332857510 |
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Enquiry
Common questions
- Is Sachtleben Chemie International GmbH FDA approved?
- Sachtleben Chemie International GmbH holds 1 FDA-registered establishment in Germany. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are Sachtleben Chemie International GmbH's drugs manufactured?
- The FDA register lists Duisburg. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, packaging.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.