Meridian Medical Technologies, 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
- 1945 Craig Road, St. Louis, Missouri (MO) 63146, United States (USA)
- Operations here
- analysislabelpack
- FDA identifiers
- FEI 1950222 · DUNS 049504624
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2024-06-05
- OAIDrug Quality Assurance2019-12-21
- OAIDrug Quality Assurance2017-03-24
- VAIDrug Quality Assurance2015-03-23
- OAIDrug Quality Assurance2014-11-25
- OAIDrug Quality Assurance2014-02-21
- OAIDrug Quality Assurance2013-10-09
- OAIDrug Quality Assurance2013-04-29
- OAIDrug Quality Assurance2013-03-04
- VAIDrug Quality Assurance2012-02-13
- NAIDrug Quality Assurance2011-05-12
- VAIDrug Quality Assurance2010-08-18
- VAIBioresearch Monitoring2009-07-31
- VAIDrug Quality Assurance2009-07-31
Drugs this plant is listed as making
3 distinct drugs across 8 products name this site in their FDA label.
- atropineMeridian Medical Technologies LLC
- atropine and pralidoxime chlorideMeridian Medical Technologies LLC
- diazepamMeridian Medical Technologies LLC
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.