Suppliers / Allergan Produtos Farmaceuticos Ltda

Allergan Produtos Farmaceuticos Ltda

Brazil Updated 9 July 2026

Allergan Produtos Farmaceuticos Ltda is a finished-dose manufacturer based in Brazil. It appears in 383 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), US FDA and DAV (Vietnam). Its GMP standing is certified by ANVISA (Brazil) and US FDA. Its most recent recorded inspection, by US FDA, closed on 3 September 2024 as NAI.

0
active US DMFs
0
valid CEPs
7
registered plants 4 with an FDA FEI number
383
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
4 of 4 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 3 September 2024 NAI US FDA
  • 28 July 2023 NAI US FDA
  • 24 March 2022 NAI US FDA
  • 24 June 2021 VAI US FDA
  • 29 July 2019 VAI US FDA
  • 27 February 2019 VAI US FDA
  • 1 February 2017 NAI US FDA
  • 28 October 2016 VAI US FDA

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

Registered plants

Site FDA FEI
SAO PAULO, Brazil Not on file
São Paulo, Brazil Not on file
GUARULHOS, Brazil Not on file
Cincinnati, United States 1523957
Irvine, United States 2011068
Waco, United States 1643525

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 172 2
US FDA 170 2
DAV (Vietnam) 14 None
MINSA (CR) 14 None
ARCSA (EC) 12 None
Health Canada 1 None

Questions about Allergan Produtos Farmaceuticos Ltda

Does Allergan Produtos Farmaceuticos Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Allergan Produtos Farmaceuticos Ltda. It does have 383 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Allergan Produtos Farmaceuticos Ltda FDA-registered?
4 sites operated by Allergan Produtos Farmaceuticos Ltda carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Allergan Produtos Farmaceuticos Ltda's last inspection go?
The most recent inspection on record closed on 3 September 2024 as NAI (No Action Indicated: nothing objectionable was found). 8 inspections are on file.
Where does Allergan Produtos Farmaceuticos Ltda manufacture?
7 registered sites are on record, in Brazil and United States (SAO Paulo, São Paulo and Guarulhos among others). Every site is listed on this page with the register it came from.
Which regulators recognise Allergan Produtos Farmaceuticos Ltda's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and US FDA. 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

  • 97 active litigation matters are on record.
  • The most recent inspection outcome was NAI, on 3 September 2024.

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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