The public registers hold a second record for EUROAPI Germany. The fuller profile, with 48 active US DMFs and 53 valid CEPs, is at EUROAPI. Figures on this page cover only this record.
EUROAPI Germany is an API manufacturer based in Germany. It holds 6 active US drug master files across a filed portfolio of 6 molecules. Its most recent recorded inspection, by US FDA, closed on 4 March 2022 as VAI.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| Germany, Germany | 3020754015 |
| Molecule | Regulators | Docs |
|---|---|---|
| Clobazam | US FDA | 1 |
| Furosemide | US FDA | 1 |
| Glimepiride | US FDA | 1 |
| Ketoprofen | US FDA | 1 |
| Leflunomide | US FDA | 1 |
| Ramipril | US FDA | 1 |
Also appears on these molecule pages
Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.
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