Suppliers / Laboratorios Liconsa

Laboratorios Liconsa

Spain 52 employees Updated 9 July 2026

Laboratorios Liconsa is a finished-dose manufacturer based in Spain. It appears in 461 regulatory filings across 16 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), MPA (SE) and DAV (Vietnam). Its GMP standing is certified by ANVISA (Brazil), EMA and FDA (GH), among 5 authorities.

0
active US DMFs
0
valid CEPs
5
registered plants
461
filings across 16 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
Guadalajara, United Arab Emirates Not on file
Guadalajara ., United Arab Emirates Not on file
AZUQUECA DE HENARES, Spain Not on file
Guadalajara, Spain Not on file
Guadalajara, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 99 None
MPA (SE) 60 None
DAV (Vietnam) 53 None
AEMPS (ES) 47 1
ARCSA (EC) 46 None
AIFA (IT) 42 None
ANVISA (Brazil) None 2
EMA None 2
FDA (GH) None 1
NAFDAC (NG) None 1

Questions about Laboratorios Liconsa

Does Laboratorios Liconsa hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Liconsa. It does have 461 filings with 16 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Liconsa manufacture?
5 registered sites are on record, in United Arab Emirates and Spain (Guadalajara, Guadalajara . and Azuqueca DE Henares among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Liconsa's GMP?
Current GMP certificates are on record from ANVISA (Brazil), EMA, FDA (GH), NAFDAC (NG) and AEMPS (ES). 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