Register entry

Kaneka Eurogentec SA

Data as of · How to read this 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
EstablishmentAddressRegistered forFEI / DUNS
Kaneka Eurogentec SARue du Bois Saint-Jean 14, Seraing, Liege B-4102, Belgium (BEL)Analytical testing, Active ingredient (API) manufacture3003323169371800140
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-GLUCARPIDASEliquid76356-101BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
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Comparable companies in Belgium

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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.