Is Tiofarma BV FDA approved?

Tiofarma BV holds 1 FDA-registered establishment in the Netherlands. 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 Tiofarma BV's drugs manufactured?

The FDA register lists Oud Beijerland. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.

Tiofarma BV

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: Netherlands

Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Tiofarma B.V.Registrant: Tiofarma BV	Hermanus Boerhaavestraat 1, Oud Beijerland, 3261 ME, Netherlands (NLD)	Analytical testing, Labelling, Finished drug manufacture, Packaging	3013984264490856367

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Common questions

Is Tiofarma BV FDA approved?: Tiofarma BV holds 1 FDA-registered establishment in the Netherlands. 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 Tiofarma BV's drugs manufactured?: The FDA register lists Oud Beijerland. Registered operations: analytical testing, 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.