Is Fermion Oy FDA approved?

Fermion Oy holds 3 FDA-registered establishments in Finland. 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 Fermion Oy's drugs manufactured?

The FDA register lists Espoo; Hanko Pohjoinen; Oulu. Registered operations: analytical testing, active ingredient (API) manufacture, labelling.

What drugs does Fermion Oy make?

20 products are listed under Fermion Oy 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.

Fermion Oy

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

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Registered sites: 3
Active NDC listings: 20
Live patents: 0
Countries: 1
Base: Finland

Authorisation

Registered operations

Analytical testing3Active ingredient (API) manufacture2Labelling2

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Fermion Oy	Koivu-Mankkaan tie 6 A, Espoo, FI-02200, Finland (FIN)	Analytical testing	3003491490401656850
Fermion Oy	Orioninkatu 2, Hanko Pohjoinen, FI-10960, Finland (FIN)	Analytical testing, Active ingredient (API) manufacture, Labelling	3002807817537993060
Fermion Oy	Laaketehtaantie 2, Oulu, FI-90660, Finland (FIN)	Analytical testing, Active ingredient (API) manufacture, Labelling	3003340711537994803

Catalogue

Drug listings by form and route

20 active NDC listings: 20 bulk ingredient. By marketing category: BULK INGREDIENT 20.

Dosage form	NDCs
powder	20

Route	NDCs

Labeller name on the listing	NDCs
fermion oy	20

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	CROMOLYN SODIUM	powder	12780-4960BULK INGREDIENT
-	Dexmedetomidine Hydrochloride	powder	12780-4640BULK INGREDIENT
-	HYDROXYCHLOROQUINE SULFATE	powder	12780-2771BULK INGREDIENT
-	IRINOTECAN HYDROCHLORIDE	powder	12780-4860BULK INGREDIENT
-	MERCAPTOPURINE	powder	12780-0299BULK INGREDIENT
-	QUETIAPINE FUMARATE	powder	12780-4930BULK INGREDIENT
-	TRILACICLIB DIHYDROCHLORIDE DIHYDRATE	powder	12780-4780BULK INGREDIENT
-	alprazolam	powder	12780-4630BULK INGREDIENT
-	azathioprine	powder	12780-0300BULK INGREDIENT
-	buspirone hydrochloride	powder	12780-2940BULK INGREDIENT
-	carbidopa	powder	12780-4420BULK INGREDIENT
-	diltiazem hydrochloride	powder	12780-2960BULK INGREDIENT
-	flutamide	powder	12780-4750BULK INGREDIENT
-	formoterol fumarate	powder	12780-4880BULK INGREDIENT
-	glipizide	powder	12780-4680BULK INGREDIENT
-	methotrexate	powder	12780-0491BULK INGREDIENT
-	methotrexate sodium	powder	12780-6690BULK INGREDIENT
-	nadolol	powder	12780-0154BULK INGREDIENT
-	propafenone hydrochloride	powder	12780-4900BULK INGREDIENT
-	tolnaftate	powder	12780-4800BULK INGREDIENT

Neighbours

Registered in the same town

Orion Corporation, Orion PharmaEspoo, FIN
Pharmatory OyOulu, FIN

Compare

Comparable companies in Finland

Orion Corporation, Orion Pharma3 sites · 3 NDC
PCAS Finland Oy1 site · 20 NDC
Pharmatory Oy1 site · 3 NDC
Oy West eSales Ab Ltd1 site · 1 NDC

Enquiry

Common questions

Is Fermion Oy FDA approved?: Fermion Oy holds 3 FDA-registered establishments in Finland. 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 Fermion Oy's drugs manufactured?: The FDA register lists Espoo; Hanko Pohjoinen; Oulu. Registered operations: analytical testing, active ingredient (API) manufacture, labelling.
What drugs does Fermion Oy make?: 20 products are listed under Fermion Oy 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.