Curia New Mexico, 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
- 4401 Alexander Blvd. NE, Albuquerque, New Mexico (NM) 87107, United States (USA)
- Operations here
- labelmanufacturepackrepack
- FDA identifiers
- FEI 1643045 · DUNS 826977121
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2024-06-28
- VAIDrug Quality Assurance2020-03-20
- VAIDrug Quality Assurance2016-12-07
- VAIDrug Quality Assurance2015-06-05
- VAIDrug Quality Assurance2014-07-17
- VAIDrug Quality Assurance2013-08-23
- VAIDrug Quality Assurance2012-04-19
- VAIDrug Quality Assurance2011-08-16
- VAIDrug Quality Assurance2010-03-12
- VAIDrug Quality Assurance2008-11-07
Drugs this plant is listed as making
1 distinct drugs across 1 products name this site in their FDA label.
- palonosetron hydrochlorideCipla USA 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.