Tolmar, 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
- 701 Centre Avenue, Fort Collins, Colorado (CO) 80526, United States (USA)
- Operations here
- analysislabelmanufacturepack
- FDA identifiers
- FEI 3006218434 · DUNS 791156578
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIBioresearch Monitoring2024-02-23
- VAIDrug Quality Assurance2023-01-31
- VAIDrug Quality Assurance2020-01-28
- VAIBioresearch Monitoring2018-04-06
- VAIDrug Quality Assurance2017-12-06
- VAIDrug Quality Assurance2016-09-20
- VAIDrug Quality Assurance2014-02-16
- VAIDrug Quality Assurance2013-05-31
- VAIBioresearch Monitoring2012-09-07
- VAIDrug Quality Assurance2012-09-07
- VAIDrug Quality Assurance2011-06-30
- VAIDrug Quality Assurance2009-12-11
Drugs this plant is listed as making
1 distinct drugs across 1 products name this site in their FDA label.
- Diclofenac SodiumAmneal Pharmaceuticals of New York 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.