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Manufacturing facility

Eurofins Lancaster Laboratories, LLC

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
United States
Registered address
2425 New Holland Pike, Lancaster, Pennsylvania (PA) 17601, United States (USA)
Operations here
analysis
FDA identifiers
FEI 2513291 · DUNS 069777290

FDA inspection history

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

  • NAIHuman Cellular, Tissue, and Gene Therapies2025-09-23
  • VAIDrug Quality Assurance2025-08-26
  • NAIBlood and Blood Products2021-10-21
  • NAIHuman Cellular, Tissue, and Gene Therapies2021-10-21
  • NAIVaccines and Allergenic Products2021-10-21
  • NAIDrug Quality Assurance2019-10-17
  • NAIHuman Cellular, Tissue, and Gene Therapies2019-09-13
  • NAIDrug Quality Assurance2017-09-28
  • NAIHuman Cellular, Tissue, and Gene Therapies2017-09-28
  • NAIDrug Quality Assurance2015-06-19
  • NAIHuman Cellular, Tissue, and Gene Therapies2014-04-14
  • NAIDrug Quality Assurance2013-06-27
  • NAIDrug Quality Assurance2012-05-17
  • NAIHuman Cellular, Tissue, and Gene Therapies2011-01-25
  • VAIDrug Quality Assurance2010-09-07
  • NAIDrug Quality Assurance2009-10-06

Drugs this plant is listed as making

12 distinct drugs across 30 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.