Zhejiang East-Asia Pharmaceutical is an API manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its filings concentrate with MINSA (CR), NAFDAC (NG) and UZPHARM (UZ). Its GMP standing is certified by MFDS (Korea).
| Site | FDA FEI |
|---|---|
| Taizhou, China | Not on file |
| Taizhou, China | Not on file |
| Pubagang, China | Not on file |
| Molecule | Regulators | Docs |
|---|---|---|
| Levofloxacin | EDQM | 1 |
| Terbinafine | EDQM | 1 |
| Trimebutine | EDQM | 1 |
Also appears on these molecule pages
| Regulator | Filings | GMP certificates |
|---|---|---|
| MINSA (CR) | 7 | None |
| NAFDAC (NG) | 3 | None |
| UZPHARM (UZ) | 1 | None |
| MFDS (Korea) | None | 4 |
Choose your molecules and target markets. Zhejiang East-Asia Pharmaceutical comes back tiered against every other supplier able to file there.
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