Register entry

Urquima, S.A.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
4
Live patents
0
Countries
1
Base
Spain
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Urquima, S.A.Arnau de Vilanova, 22-42, Sant Fost de Campsentelles (BA), 08105, Spain (ESP)Active ingredient (API) manufacture3002808432460940854
Catalogue

Drug listings by form and route

4

4 active NDC listings: 4 bulk ingredient. By marketing category: BULK INGREDIENT 4.

Dosage formNDCs
powder4
RouteNDCs
Labeller name on the listingNDCs
urquima, s.a.4
Catalogue

Marketed products

4
BrandGeneric nameForm / routeNDC
-Azelastine Hydrochloridepowder54752-0008BULK INGREDIENT
-Glipizidepowder54752-0054BULK INGREDIENT
-Ivabradine Hydrochloridepowder54752-0020BULK INGREDIENT
-Olopatadine Hydrochloridepowder54752-0006BULK INGREDIENT
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Comparable companies in Spain

Enquiry

Common questions

Is Urquima, S.A. FDA approved?
Urquima, S.A. holds 1 FDA-registered establishment in Spain. 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 Urquima, S.A.'s drugs manufactured?
The FDA register lists Sant Fost de Campsentelles (BA). Registered operations: active ingredient (API) manufacture.
What drugs does Urquima, S.A. make?
4 products are listed under Urquima, S.A. in the openFDA NDC Directory, most often as powder. 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.