Drug factory · FDA FEI 3010401502
Apertus Pharmaceuticals, LLC
331 Consort Dr, Ballwin, MO, United States
Problems found, fixed voluntarily at FDA's last inspection, Oct 31, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
2 drug inspections on record since 2020: 0 with no problems, 2 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Methenamine, Sodium Phosphate, Monobasic, Monohydrate, Phenyl Salicylate, Methyl | Makes it | Apace Packaging | 15338-502, 15338-503 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Oct 31, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jan 16, 2020 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: manufacture.