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Asahi Kasei Pharma Corporation — China drug registrations and re-registration deadlines

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

Approval numberProductCertificate expiresRe-registration deadline (Art. 82)
国药准字HJ20171046Elcitonin
依降钙素注射液
2027-04-282026-10-28
国药准字HJ20171234Exacin
硫酸异帕米星注射液
2027-08-302027-02-28
国药准字HJ20171235Exacin
硫酸异帕米星注射液
2027-08-302027-02-28
国药准字HJ20140243Bredinin
咪唑立宾片
2029-09-232029-03-23
国药准字HJ20140244Bredinin
咪唑立宾片
2029-09-232029-03-23
国药准字HJ20150252Eril
盐酸法舒地尔注射液
2030-03-182029-09-18
国药准字HJ20200016Flivas
萘哌地尔片
2030-04-142029-10-14
国药准字HJ20200017Flivas
萘哌地尔片
2030-04-142029-10-14

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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