Suppliers / Aché Laboratorios Farmacéuticos S. A

Aché Laboratorios Farmacéuticos S. A

Brazil 22 employees 2 duplicate records merged Updated 9 July 2026

Aché Laboratorios Farmacéuticos S. A is a finished-dose manufacturer based in Brazil. It appears in 1,652 regulatory filings across 6 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) and INVIMA (CO).

0
active US DMFs
0
valid CEPs
6
registered plants
1,652
filings across 6 regulators

Registered plants

Site FDA FEI
GUARULHOS, Brazil Not on file
SAO PAULO, Brazil Not on file
São Paulo, Brazil Not on file
CABO DE SANTO AGOSTINHO, Brazil Not on file
ANÁPOLIS, Brazil Not on file
Guarulhos Sao Paulo, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 1,625 9
ARCSA (EC) 13 None
MINSA (CR) 8 None
INVIMA (CO) 4 1
COFEPRIS (MX) 1 None
DIGEMAPS (DO) 1 None

Questions about Aché Laboratorios Farmacéuticos S. A

Does Aché Laboratorios Farmacéuticos S. A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Aché Laboratorios Farmacéuticos S. A. It does have 1,652 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Aché Laboratorios Farmacéuticos S. A manufacture?
6 registered sites are on record, in Brazil and Colombia (Guarulhos, SAO Paulo and São Paulo among others). Every site is listed on this page with the register it came from.
Which regulators recognise Aché Laboratorios Farmacéuticos S. A's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and INVIMA (CO). 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