Cipla Ltd. — China registrations and re-registration filing lines
5 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest filing line: 2027-08-27.
| Approval number | Product | Certificate expires | Filing line (Art. 82) |
|---|---|---|---|
| 国药准字HJ20233132 | Esomeprazole Magnesium for Delayed-Release Oral Suspension 艾司奥美拉唑镁肠溶干混悬剂 | 2028-02-27 | 2027-08-27 |
| 国药准字HJ20233133 | Esomeprazole Magnesium for Delayed-Release Oral Suspension 艾司奥美拉唑镁肠溶干混悬剂 | 2028-02-27 | 2027-08-27 |
| 国药准字HJ20233134 | Esomeprazole Magnesium for Delayed-Release Oral Suspension 艾司奥美拉唑镁肠溶干混悬剂 | 2028-02-27 | 2027-08-27 |
| 国药准字HJ20240127 | Levothyroxine Sodium Tablets 左甲状腺素钠片 | 2029-11-04 | 2029-05-04 |
| 国药准字HJ20240128 | Levothyroxine Sodium Tablets 左甲状腺素钠片 | 2029-11-04 | 2029-05-04 |
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.