Sichuan Elixir Pharmaceutical is an API manufacturer based in China. It holds 13 active US drug master files across a filed portfolio of 12 molecules. Its filings concentrate with EFDA (ET), NAFDAC (NG) and SFDA (Saudi Arabia). Its GMP standing is certified by NAFDAC (NG) and FDA (GH).
| Site | FDA FEI |
|---|---|
| Nani Daman, Nigeria | Not on file |
| Molecule | Regulators | Docs |
|---|---|---|
| Cabozantinib | US FDA | 2 |
| Abemaciclib | US FDA | 1 |
| Cabazitaxel | US FDA | 1 |
| Cytisine | US FDA | 1 |
| Darolutamide | US FDA | 1 |
| Dasatinib | US FDA | 1 |
| Indigotindisulfonate Sodium | US FDA | 1 |
| Methotrexate | US FDA | 1 |
| Nilotinib | US FDA | 1 |
| Resmetirom | US FDA | 1 |
| Sn-38 | US FDA | 1 |
| Ursodeoxycholic Acid | US FDA | 1 |
Also appears on these molecule pages
| Regulator | Filings | GMP certificates |
|---|---|---|
| EFDA (ET) | 44 | None |
| NAFDAC (NG) | 34 | 3 |
| SFDA (Saudi Arabia) | 9 | None |
| FDA (GH) | 8 | 1 |
| ZAMRA (ZM) | 3 | None |
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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