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Manufacturing facility

Eurofarma Laboratorios S/A

A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.

Country
Brazil
Registered address
Rod Presidente Castelo Branco 3565, Itapevi, SAO PAULO 06696000, Brazil (BRA)
Operations here
analysislabelmanufacturepacksterilize
FDA identifiers
FEI 3009538725 · DUNS 678788835

FDA inspection history

Outcomes of closed FDA inspections at this site, every FDA program area; the official-action banner above considers Drug Quality Assurance inspections only.

  • VAIDrug Quality Assurance2022-09-20

Drugs this plant is listed as making

1 distinct drugs across 2 products name this site for a manufacturing step (any MANUFACTURE-type role, API included). Counts are per distinct generic name (case-insensitive).

Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.