Suppliers / Eurofarma Laboratorios

Eurofarma Laboratorios

Brazil Updated 9 July 2026

Eurofarma Laboratorios is a finished-dose manufacturer based in Brazil. It appears in 3,199 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by ANVISA (Brazil), INVIMA (CO) and ISP (CL). Its most recent recorded inspection, by US FDA, closed on 20 September 2022 as VAI.

0
active US DMFs
0
valid CEPs
10
registered plants 1 with an FDA FEI number
3,199
filings across 10 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 20 September 2022 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
São Paulo, Brazil Not on file
MONTES CLAROS, Brazil Not on file
SAO PAULO, Brazil Not on file
RIBEIRAO PRETO, Brazil Not on file
ITAPEVI, Brazil Not on file
Brazil, Brazil 3009538725

4 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 2,211 11
ARCSA (EC) 414 None
MINSA (CR) 200 None
DIGEMAPS (DO) 136 None
ISP (CL) 112 1
INHRR (VE) 85 None
INVIMA (CO) None 2

Questions about Eurofarma Laboratorios

Does Eurofarma Laboratorios hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Eurofarma Laboratorios. It does have 3,199 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Eurofarma Laboratorios FDA-registered?
One site operated by Eurofarma Laboratorios carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Eurofarma Laboratorios's last inspection go?
The most recent inspection on record closed on 20 September 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Eurofarma Laboratorios manufacture?
10 registered sites are on record, in Brazil, Colombia, Mexico and Peru (São Paulo, Montes Claros and SAO Paulo among others). Every site is listed on this page with the register it came from.
Which regulators recognise Eurofarma Laboratorios's GMP?
Current GMP certificates are on record from ANVISA (Brazil), INVIMA (CO) and ISP (CL). 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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Open risk flags

  • The most recent inspection outcome was VAI, on 20 September 2022.

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Abbott Laboratorios Do Brasil Ltda also in Brazil Aché Laboratorios Farmacéuticos S. A also in Brazil Alcon Laboratórios Do Brasil Ltda also in Brazil Allergan Produtos Farmaceuticos Ltda also in Brazil Baxter Hospitalar Ltda also in Brazil

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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