Greer Laboratories, 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
- 639 Nuway Circle, NE, PO Box 800, Lenoir, North Carolina (NC) 28645, United States (USA)
- Operations here
- manufacture
- FDA identifiers
- FEI 1011574 · DUNS 024671414
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2025-12-12
- VAIVaccines and Allergenic Products2025-12-12
- VAIVaccines and Allergenic Products2024-12-18
- VAIVaccines and Allergenic Products2019-09-11
- VAIVaccines and Allergenic Products2017-11-22
- VAIVaccines and Allergenic Products2015-08-27
- NAIDrug Quality Assurance2014-03-12
- NAIDrug Quality Assurance2012-02-15
- NAIVaccines and Allergenic Products2011-12-07
- NAIDrug Quality Assurance2010-06-29
- VAIVaccines and Allergenic Products2009-03-27
Drugs this plant is listed as making
3 distinct drugs across 7 products name this site in their FDA label.
- Dermatophagoides farinaeGreer Laboratories, Inc.
- Dermatophagoides farinae and Dermatophagoides pteronyssinusGreer Laboratories, Inc.
- Dermatophagoides pteronyssinusGreer Laboratories, 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.