Is GP PHARM S.A.U. FDA approved?

GP PHARM S.A.U. holds 1 FDA-registered establishment in Spain. 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 GP PHARM S.A.U.'s drugs manufactured?

The FDA register lists SANT QUINTI DE MEDIONA. Registered operations: analytical testing, labelling, finished drug manufacture, packaging, sterilize.

What drugs does GP PHARM S.A.U. make?

2 products are listed under GP PHARM S.A.U. in the openFDA NDC Directory, most often as injection, powder, lyophilized, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

GP PHARM S.A.U.

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

Request a quote Claim this profile

Registered sites: 1
Active NDC listings: 2
Live patents: 0
Countries: 1
Base: Spain

Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1sterilize1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
GP PHARM S.A.U.	POLIGONO INDUSTRIAL ELS VINYETS-FOGARS (SECTOR II), CR C-244 KM 22, SANT QUINTI DE MEDIONA, - 08777, Spain (ESP)	Analytical testing, Labelling, Finished drug manufacture, Packaging, sterilize	3008345811462006581

Catalogue

Drug listings by form and route

2 active NDC listings: 2 drug for further processing. By marketing category: DRUG FOR FURTHER PROCESSING 2.

Dosage form	NDCs
injection, powder, lyophilized, for solution	2

Route	NDCs

Labeller name on the listing	NDCs
gp pharm sa	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	LURBINECTEDIN	injection, powder, lyophilized, for solution	69112-102DRUG FOR FURTHER PROCESSING
-	cetrorelix acetate	injection, powder, lyophilized, for solution	69112-103DRUG FOR FURTHER PROCESSING

Neighbours

Registered in the same town

BCN Peptides SASANT QUINTI DE MEDIONA, ESP

Compare

Comparable companies in Spain

QUIMICA SINTETICA SA1 site · 58 NDC
Derivados Quimicos SAU1 site · 38 NDC
Interquim, S.A.1 site · 26 NDC
Farmhispania S.A.1 site · 17 NDC
Rolabo Outsourcing S.L.1 site · 9 NDC
AGC Pharma Chemicals Europe, S.L.U .1 site · 7 NDC
BERIOSKA SL1 site · 7 NDC
Ercros SA1 site · 7 NDC
Towa Pharmaceutical Europe, S.L.1 site · 6 NDC
Quality Chemicals S.L.1 site · 3 NDC

Enquiry

Common questions

Is GP PHARM S.A.U. FDA approved?: GP PHARM S.A.U. holds 1 FDA-registered establishment in Spain. 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 GP PHARM S.A.U.'s drugs manufactured?: The FDA register lists SANT QUINTI DE MEDIONA. Registered operations: analytical testing, labelling, finished drug manufacture, packaging, sterilize.
What drugs does GP PHARM S.A.U. make?: 2 products are listed under GP PHARM S.A.U. in the openFDA NDC Directory, most often as injection, powder, lyophilized, for solution. 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.