Quality Chemical Laboratories
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
- 3400 Enterprise Drive, Wilmington, North Carolina (NC) 28405, United States (USA)
- Operations here
- analysisapi manufacturemanufacturepack
- FDA identifiers
- FEI 3002323490 · DUNS 071344167
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- NAIVaccines and Allergenic Products2025-07-24
- VAIDrug Quality Assurance2024-11-20
- VAIDrug Quality Assurance2017-07-27
- VAIDrug Quality Assurance2013-09-26
- VAIDrug Quality Assurance2010-08-24
- NAIDrug Quality Assurance2010-04-01
Drugs this plant is listed as making
4 distinct drugs across 4 products name this site in their FDA label.
- amifampridine phosphateCatalyst Pharmaceuticals, Inc.
- Eflornithine HydrochlorideUswm, Llc
- ensifentrineMerck Sharp & Dohme Llc
- Irinotecan HydrochlorideIpsen Biopharmaceuticals, 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.