Takeda Pharmaceuticals U.S.A., Inc. — China drug registrations and re-registration deadlines
8 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2028-05-01.
| Approval number | Product | Certificate expires | Re-registration deadline (Art. 82) |
|---|---|---|---|
| 国药准字SJ20181006 | FLEXBUMIN 人血白蛋白 | 2028-11-01 | 2028-05-01 |
| 国药准字SJ20181007 | FLEXBUMIN 人血白蛋白 | 2028-11-01 | 2028-05-01 |
| 国药准字SJ20247007 | FLEXBUMIN 人血白蛋白 | 2028-11-01 | 2028-05-01 |
| 国药准字HJ20230146 | Maribavir Tablets 马立巴韦片 | 2028-12-18 | 2028-06-18 |
| 国药准字SJ20240009 | OBIZUR 注射用舒索凝血素α | 2029-02-19 | 2028-08-19 |
| 国药准字SJ20240032 | VONVENDI 注射用伏尼凝血素α | 2029-07-29 | 2029-01-29 |
| 国药准字SJ20240033 | VONVENDI 注射用伏尼凝血素α | 2029-07-29 | 2029-01-29 |
| 国药准字SJ20200025 | TAKHZYRO 拉那利尤单抗注射液 | 2031-04-26 | 2030-10-26 |
Under the Provisions for Drug Registration (药品注册管理办法) Art. 82, an application to renew an overseas-manufactured drug registration is filed with the Center for Drug Evaluation no later than 6 months before the certificate expires; the filing line column is that arithmetic applied to the expiry cell. Art. 84(1): a certificate with no application by expiry is not re-registered and is cancelled at expiry. Every figure is taken from the public NMPA database as of 2026-06-28, or computed from it. Registration data changes; the NMPA portal governs. This page states no view on whether any of these products' Domestic Responsible Person (境内责任人) arrangements meet NMPA Announcement No. 137 — that cannot be determined from a public entry.