Allergan Produtos Farmaceuticos Ltda is a finished-dose manufacturer based in United States. 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 MINSA (CR). 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.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| São Paulo, Brazil | Not on file |
| SAO PAULO, Brazil | Not on file |
| GUARULHOS, Brazil | Not on file |
| Irvine, United States | 2011068 |
| Campbell, United States | 3000720089 |
| Cincinnati, United States | 1523957 |
1 further sites are on record.
| Regulator | Filings | GMP certificates |
|---|---|---|
| ANVISA (Brazil) | 172 | 2 |
| US FDA | 170 | 2 |
| MINSA (CR) | 14 | None |
| DAV (Vietnam) | 14 | None |
| ARCSA (EC) | 12 | None |
| Health Canada | 1 | None |
Choose your molecules and target markets. Allergan Produtos Farmaceuticos Ltda comes back tiered against every other supplier able to file there.
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