Lek Pharmaceuticals d.d. — China drug registrations and re-registration deadlines
5 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2027-04-24.
| Approval number | Product | Certificate expires | Re-registration deadline (Art. 82) |
|---|---|---|---|
| 国药准字HJ20180007 | Rosuvastatin Calcium Tablets 瑞舒伐他汀钙片 | 2027-10-24 | 2027-04-24 |
| 国药准字HJ20180008 | Rosuvastatin Calcium Tablets 瑞舒伐他汀钙片 | 2027-10-24 | 2027-04-24 |
| 国药准字HJ20220084 | Mometasone Furoate Aqueous Nasal Spray 糠酸莫米松鼻喷雾剂 | 2027-11-14 | 2027-05-14 |
| 国药准字HJ20220085 | Mometasone Furoate Aqueous Nasal Spray 糠酸莫米松鼻喷雾剂 | 2027-11-14 | 2027-05-14 |
| 国药准字HJ20150007 | Amlodipine Besylate Tablets 苯磺酸氨氯地平片 | 2030-10-19 | 2030-04-19 |
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.