GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LTD ENGLAND — China drug registrations and re-registration deadlines
2 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2029-01-22.
| Approval number | Product | Certificate expires | Re-registration deadline (Art. 82) |
|---|---|---|---|
| 国药准字HJ20190055 | Fluticasone Furoate, Umeclidinium Bromide and Vilanterol Trifenatate Powder for Inhalation 氟替美维吸入粉雾剂 | 2029-07-22 | 2029-01-22 |
| 国药准字HJ20260003 | Fluticasone Furoate, Umeclidinium Bromide and Vilanterol Trifenatate Powder for Inhalation 氟替美维吸入粉雾剂 | 2031-01-13 | 2030-07-13 |
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.