Register entry
- Registered sites
- 2
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 2
- Base
- Switzerland
Authorisation
Registered operations
Analytical testing2Labelling2Finished drug manufacture2Packaging2
Sites
Registered establishments
2| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Rommelag CDMO Switzerland AG | Industriestrasse Briseck 4, Zell LU, LUZERN 6144, Switzerland (CHE) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 3004079469481488112 |
| Rommelag CDMO GmbH | Bahnhofstr. 20, Abtsgmund-Untergroningen, 73453, Germany (DEU) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 3002808845313222457 |
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Enquiry
Common questions
- Is Rommelag CDMO Switzerland AG FDA approved?
- Rommelag CDMO Switzerland AG holds 2 FDA-registered establishments across 2 countries. 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 Rommelag CDMO Switzerland AG's drugs manufactured?
- At registered sites in Switzerland, Germany. The FDA register lists Zell LU; Abtsgmund-Untergroningen. Registered operations: analytical testing, labelling, finished drug manufacture, 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.