SinoReg

Fresenius Kabi Deutschland GmbH — China drug registrations and re-registration deadlines

18 certificates in the NMPA overseas-manufactured drug database (境外生产药品库), snapshot 2026-06-28. Earliest re-registration deadline: 2028-12-10.

Approval numberProductCertificate expiresRe-registration deadline (Art. 82)
国药准字HJ20240040Linezolid and Glucose Injection
利奈唑胺葡萄糖注射液
2029-06-102028-12-10
国药准字HJ20150654Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150655Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150656Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150657Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150658Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150659Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150660Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150661Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150662Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20150663Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20160360Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20160671Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20171120Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20181145Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20181223Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20191011Propofol Medium and Long Chain Fat Emulsion Injection
丙泊酚中/长链脂肪乳注射液
2030-03-312029-09-30
国药准字HJ20210060Multi-trace Elements Injection (III)
多种微量元素注射液(Ⅲ)
2031-03-012030-09-01

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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