Is UAB Teva Baltics FDA approved?

UAB Teva Baltics holds 1 FDA-registered establishment in Lithuania. 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 UAB Teva Baltics's drugs manufactured?

The FDA register lists Vilnius. Registered operations: analytical testing, active ingredient (API) manufacture.

UAB Teva Baltics

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: Lithuania

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
UAB Teva Baltics	Moletu pl. 5, Vilnius, LT-08409, Lithuania (LTU)	Analytical testing, Active ingredient (API) manufacture	3008110727565487722

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Common questions

Is UAB Teva Baltics FDA approved?: UAB Teva Baltics holds 1 FDA-registered establishment in Lithuania. 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 UAB Teva Baltics's drugs manufactured?: The FDA register lists Vilnius. Registered operations: analytical testing, active ingredient (API) manufacture.

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.