Drug factory · FDA FEI 3002808295
Corden Pharma Chenove
47 rue de Longvic, Chenove, France
Problems found, fixed voluntarily at FDA's last inspection, Feb 14, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
5 drug inspections on record since 2009: 1 with no problems, 4 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Tetrabenazine | Makes the active ingredient | Lundbeck Pharmaceuticals LLC | 67386-421, 67386-422 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Feb 14, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Sep 13, 2019 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Aug 26, 2016 | No problems found | Drug Quality Assurance | — |
| Mar 14, 2014 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Nov 20, 2009 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: api manufacture.