Takeda Manufacturing Austria AG — China drug registrations and re-registration deadlines
6 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2027-01-28.
| Approval number | Product | Certificate expires | Re-registration deadline (Art. 82) |
|---|---|---|---|
| 国药准字SJ20170020 | ADVATE 注射用重组人凝血因子Ⅷ | 2027-07-28 | 2027-01-28 |
| 国药准字SJ20170021 | ADVATE 注射用重组人凝血因子Ⅷ | 2027-07-28 | 2027-01-28 |
| 国药准字SJ20170022 | ADVATE 注射用重组人凝血因子Ⅷ | 2027-07-28 | 2027-01-28 |
| 国药准字SJ20170023 | ADVATE 注射用重组人凝血因子Ⅷ | 2027-07-28 | 2027-01-28 |
| 国药准字SJ20180020 | Human Albumin 人血白蛋白 | 2028-02-19 | 2027-08-19 |
| 国药准字SJ20160018 | Human Albumin 人血白蛋白 | 2028-03-20 | 2027-09-20 |
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.