Is Nordmark Pharma GmbH FDA approved?

Nordmark Pharma GmbH holds 1 FDA-registered establishment in Germany. 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 Nordmark Pharma GmbH's drugs manufactured?

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

What drugs does Nordmark Pharma GmbH make?

1 product is listed under Nordmark Pharma GmbH 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.

Nordmark Pharma GmbH

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

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

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Nordmark Pharma GmbH	Pinnauallee 4, Uetersen, Schleswig-Holstein D-25436, Germany (DEU)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging	3003293533332430201

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Thyroid, Porcine	powder	81618-0004BULK INGREDIENT

Neighbours

Registered in the same town

Norbitec GmbHUetersen, DEU

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Common questions

Is Nordmark Pharma GmbH FDA approved?: Nordmark Pharma GmbH holds 1 FDA-registered establishment in Germany. 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 Nordmark Pharma GmbH's drugs manufactured?: The FDA register lists Uetersen. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does Nordmark Pharma GmbH make?: 1 product is listed under Nordmark Pharma GmbH 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.