Is PCAS Finland Oy FDA approved?

PCAS Finland Oy holds 1 FDA-registered establishment 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 PCAS Finland Oy's drugs manufactured?

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

What drugs does PCAS Finland Oy make?

20 products are listed under PCAS Finland 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.

PCAS Finland Oy

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

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

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
PCAS Finland Oy	Messukent�nkatu 8, TURKU, 20210, Finland (FIN)	Analytical testing, Active ingredient (API) manufacture	3003469991369587311

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
pcas finland oy	12
pcas finland oy	6
pcas finland	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	APRACLONIDINE HYDROCHLORIDE	powder	51014-7782BULK INGREDIENT
-	ARTICAINE HCl	powder	51014-7872BULK INGREDIENT
-	BACLOFEN	powder	51014-7035BULK INGREDIENT
-	CICLOPIROX	powder	51014-7851BULK INGREDIENT
-	CLONIDINE BASE	powder	51014-7544BULK INGREDIENT
-	CLONIDINE HCl	powder	51014-7543BULK INGREDIENT
-	Cinacalcet HCI	powder	51014-7101BULK INGREDIENT
-	Clonidine Base Micronized	powder	51014-7944BULK INGREDIENT
-	DESIPRAMINE HCl	powder	51014-7943BULK INGREDIENT
-	DISOPYRAMIDE PHOSPHATE	powder	51014-7863BULK INGREDIENT
-	DORZOLAMIDE HCl	powder	51014-7777BULK INGREDIENT
-	GLYCOPYRROLATE	powder	51014-7146BULK INGREDIENT
-	Hemin	powder	51014-7945BULK INGREDIENT
-	OLOPATADINE HCL	powder	51014-7733BULK INGREDIENT
-	R-BACLOFEN	powder	51014-7430BULK INGREDIENT
-	TAZAROTENE	powder	51014-7755BULK INGREDIENT
-	TIMOLOL HEMIHYDRATE	powder	51014-7520BULK INGREDIENT
-	TIMOLOL MALEATE	powder	51014-7510BULK INGREDIENT
-	Tetrahydrozoline HCI	powder	51014-7162BULK INGREDIENT
-	Timolol Maleate (7125)	powder	51014-7125BULK INGREDIENT

Neighbours

Registered in the same town

Bayer Healthcare Manufacturing SrlTurku, FIN
Orion Corporation, Orion PharmaTurku, FIN

Compare

Comparable companies in Finland

Pharmatory Oy1 site · 3 NDC
Oy West eSales Ab Ltd1 site · 1 NDC
Fermion Oy3 sites · 20 NDC
Orion Corporation, Orion Pharma3 sites · 3 NDC

Enquiry

Common questions

Is PCAS Finland Oy FDA approved?: PCAS Finland Oy holds 1 FDA-registered establishment 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 PCAS Finland Oy's drugs manufactured?: The FDA register lists TURKU. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does PCAS Finland Oy make?: 20 products are listed under PCAS Finland 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.