Is Provita Eurotech Ltd FDA approved?

Provita Eurotech Ltd holds 1 FDA-registered establishment in the United Kingdom. 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 Provita Eurotech Ltd's drugs manufactured?

The FDA register lists Omagh. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.

Provita Eurotech Ltd

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 0
Live patents: 0
Countries: 1
Base: United Kingdom

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Provita Eurotech Ltd	21 Bankmore Road, Omagh, Co Tyrone BT79 0EU, United Kingdom (GBR)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging	3003114347238318232

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Common questions

Is Provita Eurotech Ltd FDA approved?: Provita Eurotech Ltd holds 1 FDA-registered establishment in the United Kingdom. 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 Provita Eurotech Ltd's drugs manufactured?: The FDA register lists Omagh. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.

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.