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Gedeon Richter Plc. — China drug registrations and re-registration deadlines

10 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2026-10-13.

Approval numberProductCertificate expiresRe-registration deadline (Art. 82)
国药准字HJ20170208Vinpocetine Injection
长春西汀注射液
2027-04-132026-10-13
国药准字HJ20220070Drospirenone and Ethinylestradiol Tablets
屈螺酮炔雌醇片
2027-08-092027-02-09
国药准字HJ20230049Desogestrel and Ethinylestradiol Tablets
去氧孕烯炔雌醇片
2028-05-112027-11-11
国药准字HJ20130595PANANGIN
门冬氨酸钾镁片
2028-10-292028-04-29
国药准字HJ20140053Postinor-2
左炔诺孕酮片
2028-11-292028-05-29
国药准字HJ20130590PANANGIN
门冬氨酸钾镁注射液
2028-12-242028-06-24
国药准字HJ20130774Vinpocetine Tablets
长春西汀片
2029-02-282028-08-28
国药准字HJ20140728Levonorgestrel Tablets
左炔诺孕酮片
2029-10-212029-04-21
国药准字HJ20250109Estradiol Transdermal Spray
雌二醇透皮喷雾剂
2030-09-082030-03-08
国药准字HJ20160170Bromocriptin-Richter
甲磺酸溴隐亭片
2031-01-062030-07-06

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.

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