Suppliers / Eurodrug Laboratories

Eurodrug Laboratories

Netherlands 98 employees Updated 9 July 2026

Eurodrug Laboratories is a finished-dose manufacturer based in Netherlands. It appears in 47 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with RAMA (GE), HSA (SG) and NPRA (MY). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
47
filings across 4 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
Toluca, Mexico Not on file
'S-GRAVENHAGE, Netherlands Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 17 None
HSA (SG) 16 None
NPRA (MY) 13 None
INVIMA (CO) 1 None
EMA None 1

Questions about Eurodrug Laboratories

Does Eurodrug Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Eurodrug Laboratories. It does have 47 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Eurodrug Laboratories manufacture?
2 registered sites are on record, in Mexico and Netherlands (Toluca and 's-gravenhage). Every site is listed on this page with the register it came from.
Which regulators recognise Eurodrug Laboratories's GMP?
Current GMP certificates are on record from 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