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Manufacturing facility

Wyeth Lederle SRL

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
Italy
Registered address
Via Franco Gorgone, Catania, 95121, Italy (ITA)
Operations here
analysislabelmanufacturepack
FDA identifiers
FEI 3002806766 · DUNS 542812040

FDA inspection history

Outcomes of closed FDA inspections at this site (drug and biologic program areas).

  • VAIDrug Quality Assurance2022-01-21
  • VAIDrug Quality Assurance2017-04-20
  • OAIDrug Quality Assurance2014-11-14
  • OAIDrug Quality Assurance2012-07-20
  • NAIDrug Quality Assurance2009-12-04

Drugs this plant is listed as making

2 distinct drugs across 3 products name this site in their FDA label.

  • temsirolimusWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
  • TigecyclineWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

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.