Suppliers / Eumedica Pharmaceuticals Industries Sl

Eumedica Pharmaceuticals Industries Sl

Spain 14 employees Updated 9 July 2026

Eumedica Pharmaceuticals Industries Sl is an API manufacturer based in Spain. It holds 2 active US drug master files and one valid CEP across a filed portfolio of 2 molecules. Its GMP standing is certified by AEMPS (ES) and EMA.

2
active US DMFs
1
valid CEPs
3
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
S.L. Llanera, Spain Not on file
Asturias, Spain Not on file
Llanera, Spain Not on file

What they file, and where

Molecule Regulators Docs
Sulbactam EDQM, US FDA 2
Ampicillin US FDA 1

Also appears on these molecule pages

Ampicillin API Sulbactam API

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) None 1
EMA None 1

Questions about Eumedica Pharmaceuticals Industries Sl

Does Eumedica Pharmaceuticals Industries Sl hold a US DMF or a CEP?
Eumedica Pharmaceuticals Industries Sl holds 2 active US drug master files and 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Eumedica Pharmaceuticals Industries Sl manufacture?
3 registered sites are on record, in Spain (S.l. Llanera, Asturias and Llanera). Every site is listed on this page with the register it came from.
What does Eumedica Pharmaceuticals Industries Sl make?
2 molecules are on record against Eumedica Pharmaceuticals Industries Sl, including Sulbactam and Ampicillin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Eumedica Pharmaceuticals Industries Sl's GMP?
Current GMP certificates are on record from AEMPS (ES) and EMA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates