Suppliers / Abbott Laboratorios Do Brasil Ltda

Abbott Laboratorios Do Brasil Ltda

Brazil Updated 9 July 2026

Abbott Laboratorios Do Brasil Ltda is a finished-dose manufacturer based in Brazil. It appears in 531 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), INFARMED (PT) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
4
registered plants
531
filings across 6 regulators

Registered plants

Site FDA FEI
São Paulo, Brazil Not on file
SAO PAULO, Brazil Not on file
RIO DE JANEIRO, Brazil Not on file
Azambuja, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 416 3
INFARMED (PT) 89 None
ARCSA (EC) 11 None
DIGEMAPS (DO) 7 None
MINSA (CR) 7 None
INVIMA (CO) 1 None

Questions about Abbott Laboratorios Do Brasil Ltda

Does Abbott Laboratorios Do Brasil Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Abbott Laboratorios Do Brasil Ltda. It does have 531 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Abbott Laboratorios Do Brasil Ltda manufacture?
4 registered sites are on record, in Brazil and Portugal (São Paulo, SAO Paulo and RIO DE Janeiro among others). Every site is listed on this page with the register it came from.
Which regulators recognise Abbott Laboratorios Do Brasil Ltda's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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