Register 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| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Hanseler AG | Industriestrasse 35, Herisau, 9100, Switzerland (CHE) | Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging | 3004136153480534130 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Olbas Analgesic Salve | salve | 69955-5005BULK INGREDIENT |
Compare
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- SINTETICA S.A.1 site · 9 NDC
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Enquiry
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.