SinoReg

Grand Medical Pty Ltd. — 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: 2030-10-12.

Approval numberProductCertificate expiresRe-registration deadline (Art. 82)
国药准字HJ20210033Indacaterol Acetate, Glycopyrronium Bromide and Mometasone Furoate Powder for Inhalation(Ⅰ)
茚达格莫吸入粉雾剂(Ⅰ)
2031-04-122030-10-12
国药准字HJ20210034Indacaterol Acetate, Glycopyrronium Bromide and Mometasone Furoate Powder for Inhalation(II)
茚达格莫吸入粉雾剂(II)
2031-04-122030-10-12
国药准字HJ20210046Indacaterol Acetate and Mometasone Furoate Powder for Inhalation(Ⅰ)
茚达特罗莫米松吸入粉雾剂(Ⅰ)
2031-05-052030-11-05
国药准字HJ20210047Indacaterol Acetate and Mometasone Furoate Powder for Inhalation(III)
茚达特罗莫米松吸入粉雾剂(III)
2031-05-052030-11-05
国药准字HJ20210048Indacaterol Acetate and Mometasone Furoate Powder for Inhalation(Ⅱ)
茚达特罗莫米松吸入粉雾剂(Ⅱ)
2031-05-052030-11-05

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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