Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Belgium
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Kaneka Eurogentec SA | Rue du Bois Saint-Jean 14, Seraing, Liege B-4102, Belgium (BEL) | Analytical testing, Active ingredient (API) manufacture | 3003323169371800140 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | GLUCARPIDASE | liquid | 76356-101BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING |
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Enquiry
Common questions
- Is Kaneka Eurogentec SA FDA approved?
- Kaneka Eurogentec SA holds 1 FDA-registered establishment in Belgium. 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 Kaneka Eurogentec SA's drugs manufactured?
- The FDA register lists Seraing. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does Kaneka Eurogentec SA make?
- 1 product is listed under Kaneka Eurogentec SA in the openFDA NDC Directory, most often as liquid. 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.