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Manufacturing facility

Sanofi-Aventis Deutschland GmbH

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
Germany
Registered address
Brüningstr. 50, Frankfurt am Main, 65926, Germany (DEU)
Operations here
analysisapi manufacturelabelmanufacturepack
FDA identifiers
FEI 3003195501 · DUNS 313218430

FDA inspection history

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

  • VAIDrug Quality Assurance2022-03-25
  • VAIDrug Quality Assurance2019-05-14
  • VAIDrug Quality Assurance2017-03-03
  • VAIDrug Quality Assurance2015-06-26
  • NAIDrug Quality Assurance2013-12-05
  • VAIDrug Quality Assurance2013-07-02
  • NAIDrug Quality Assurance2012-04-30
  • VAIDrug Quality Assurance2011-07-14
  • OAIDrug Quality Assurance2010-09-16
  • VAIDrug Quality Assurance2008-10-31

Drugs this plant is listed as making

18 distinct drugs across 44 products name this site in their FDA label.

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.

Sanofi-Aventis Deutschland GmbH — facility profile · DrugDashboards