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Manufacturing facility

Hikma Pharmaceuticals USA Inc.

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
2 Esterbrook Lane, Cherry Hill, New Jersey (NJ) 08003, United States (USA)
Operations here
analysisapi manufacturelabelmanufacturepackrelabelrepacksalvage
FDA identifiers
FEI 2220525 · DUNS 946499746

FDA inspection history

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

  • NAIDrug Quality Assurance2026-05-13
  • VAIDrug Quality Assurance2024-06-12
  • VAIDrug Quality Assurance2023-11-03
  • NAIDrug Quality Assurance2022-07-07
  • VAIDrug Quality Assurance2019-09-10
  • NAIDrug Quality Assurance2018-09-14
  • NAIDrug Quality Assurance2017-04-04
  • NAIDrug Quality Assurance2015-05-21
  • NAIUnapproved and Misbranded Drugs2014-09-19
  • NAIDrug Quality Assurance2014-05-01
  • NAIDrug Quality Assurance2013-10-22
  • VAIDrug Quality Assurance2013-06-14
  • NAIDrug Quality Assurance2013-03-28
  • NAIDrug Quality Assurance2012-10-24
  • VAIDrug Quality Assurance2011-04-13
  • VAIDrug Quality Assurance2010-10-29
  • NAIDrug Quality Assurance2010-03-11
  • VAIDrug Quality Assurance2009-03-10

Drugs this plant is listed as making

27 distinct drugs across 75 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.