Register entry

Rommelag CDMO Switzerland AG

Data as of · How to read this 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
EstablishmentAddressRegistered forFEI / DUNS
Rommelag CDMO Switzerland AGIndustriestrasse Briseck 4, Zell LU, LUZERN 6144, Switzerland (CHE)Analytical testing, Labelling, Finished drug manufacture, Packaging3004079469481488112
Rommelag CDMO GmbHBahnhofstr. 20, Abtsgmund-Untergroningen, 73453, Germany (DEU)Analytical testing, Labelling, Finished drug manufacture, Packaging3002808845313222457
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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.