Register entry

Hanseler AG

Data as of · How to read this entry

Registered sites
1
Active NDC listings
1
Live patents
0
Countries
1
Base
Switzerland
Authorisation

Registered operations

Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Hanseler AGIndustriestrasse 35, Herisau, 9100, Switzerland (CHE)Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging3004136153480534130
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-Olbas Analgesic Salvesalve69955-5005BULK INGREDIENT
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Common questions

Is Hanseler AG FDA approved?
Hanseler AG holds 1 FDA-registered establishment in Switzerland. 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 Hanseler AG's drugs manufactured?
The FDA register lists Herisau. Registered operations: active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does Hanseler AG make?
1 product is listed under Hanseler AG in the openFDA NDC Directory, most often as salve. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

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.