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.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| SAO PAULO, Brazil | Not on file |
| ITAPEVI, Brazil | Not on file |
| MONTES CLAROS, Brazil | Not on file |
| RIBEIRAO PRETO, Brazil | Not on file |
| São Paulo, Brazil | Not on file |
| Brazil, Brazil | 3009538725 |
4 further sites are on record.
| 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 |
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