Moxifloxacin Hydrochloride Eye Drops / 盐酸莫西沙星滴眼液
国药准字HJ20180089 · 眼用制剂
Re-registration deadline: 2028-01-03
The certificate expires 2028-07-03. Under the Provisions for Drug Registration (药品注册管理办法) Art. 82, an application to renew is filed no later than 6 months before expiry.
| Approval number (批准文号) | 国药准字HJ20180089 |
|---|---|
| Generic name (通用名) | Moxifloxacin Hydrochloride Eye Drops 盐酸莫西沙星滴眼液 |
| Marketing Authorisation Holder (上市许可持有人) | Novartis Pharmaceuticals Corporation United States |
| Certificate valid until (有效期至) | 2028-07-03 |
| Re-registration deadline, Art. 82 (法定申报时限) | 2028-01-03 |
| Data as of (数据快照日) | 2026-06-28 |
All China registrations held by Novartis Pharmaceuticals Corporation →
Check another product →Every figure above is taken from the public NMPA overseas-drug database (境外生产药品库) as of 2026-06-28, or computed from it under Art. 82. Registration data changes; the NMPA portal governs. This page states no view on whether this product’s Domestic Responsible Person (境内责任人) arrangement meets NMPA Announcement No. 137 — that cannot be determined from a single public entry.