Sichuan Elixir Pharmaceutical
Nigeria Updated 9 July 2026
Sichuan Elixir Pharmaceutical is an API manufacturer based in Nigeria. 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).
98
filings
across 5 regulators
Registered plants
| Site | FDA FEI |
| Nani Daman, Nigeria | Not on file |
What they file, and where
| 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 |
Show all 12 molecules on file
Also appears on these molecule pages
Filings and GMP by regulator
| 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 |
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Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates