Nomax, 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
- 9735 Green Park Industrial Drive, Saint Louis, Missouri (MO) 63123, United States (USA)
- Operations here
- manufacture
- FDA identifiers
- FEI 1937310 · DUNS 103220273
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2022-12-02
- VAIDrug Quality Assurance2018-02-01
- VAIDrug Quality Assurance2016-10-27
- VAIDrug Quality Assurance2012-01-31
- VAIDrug Quality Assurance2011-03-25
- NAIDrug Quality Assurance2010-07-26
Drugs this plant is listed as making
4 distinct drugs across 13 products name this site in their FDA label.
- Fluorescein SodiumNomax Inc.
- Potassium BicarbonateNomax Inc.
- Rose Bengal SodiumNomax 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.