Recorded Chinese product: 诺氟沙星乳膏诺氟沙星乳膏
This is a medicine registration record from NMPA data.本页为国家药监局药品注册记录。
Labeled sections from the recorded Chinese source are included below. English wording is a reference translation when one is on file, not an official English label.本记录未接入产品级适应症/安全性标注字段。
生产企业Manufacturer
- 上海通用药业股份有限公司Chinese legal name: 上海通用药业股份有限公司
主要成分Active Ingredients
- 诺氟沙星Nuofu Shaxing
药物知识说明
诺氟沙星是一种在国家药监局注册认定的药品。该药品含有诺氟沙星-0913cfff等成分。
该药品关联的活性成分包括：诺氟沙星Nuofu Shaxing。这些成分信息来自国家药监局数据库。
该药品标注的生产企业为：上海通用药业股份有限公司Chinese legal name: 上海通用药业股份有限公司。
您可以探索含有相同成分的其他药品：诺氟沙星-0913cfff成分药品。
本页面内容来自国家药监局数据库，MedicineGraph在此基础上提供关系图谱和知识导航。
Medicine Knowledge
This medicine (original name: 诺氟沙星乳膏) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 诺氟沙星Nuofu Shaxing.
Manufacturers recorded for this product: 上海通用药业股份有限公司Chinese legal name: 上海通用药业股份有限公司.
Explore other medicines containing the same ingredient: 诺氟沙星 productsProducts containing this recorded ingredient.
Source: MedicineGraph authoritative database. Relationships derived from registered product information.
这是什么What is this
- 通用名/品名Recorded product name: 诺氟沙星乳膏Recorded Chinese product: 诺氟沙星乳膏
- 剂型Dosage form: 乳膏剂Cream
- 规格Specification: 10g:0.1g。10 g:0.1 g
本段仅展示注册/说明书已记录的身份属性，不含适应症或用法建议。Identity attributes from registration/leaflet records only; no indications or usage advice.
主要成分Ingredients
生产企业Manufacturer
- 上海通用药业股份有限公司Chinese legal name: 上海通用药业股份有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H10983179
关联实体Relationships
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据及已接入说明书字段。National Medical Products Administration (China) medicine-registration data and linked leaflet fields.
- 品名来源Name source: 10多万条药品说明书数据库 (HIGH)Package-insert database (more than 100,000 records) (HIGH)
- 生产企业来源Manufacturer source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
- 剂型来源Dosage-form source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。不含适应症/安全性推断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence. No inferred indications/safety.
本段为已核准说明书原文摘录（非改写、非AI摘要），非正式英文标签，亦不构成用药建议。 Not an official English label and not medical advice. English wording, when shown, is a reference translation of the Chinese source label.
English translation for reference. Translated from the Chinese source label. Not an official English label and not medical advice.
NMPA approval number
国药准字H10983179
Manufacturer
Chinese legal name: 上海通用药业股份有限公司 (domestically manufactured)
Indications
English translation unavailable. The original Chinese source label remains available below.
Dosage and administration
English translation unavailable. The original Chinese source label remains available below.
Adverse reactions
English translation unavailable. The original Chinese source label remains available below.
Contraindications
English translation unavailable. The original Chinese source label remains available below.
Precautions
English translation unavailable. The original Chinese source label remains available below.
Storage
English translation unavailable. The original Chinese source label remains available below.
Specification
English translation unavailable. The original Chinese source label remains available below.
中文说明书原文Original Chinese source label
批准文号
国药准字H10983179
生产企业
上海通用药业股份有限公司(国产)
适应症
本品用于敏感菌所致的皮肤软组织感染，如脓疱疮、湿疹感染、足疣感染、毛囊炎、疖肿等。本品可控制烧伤肉芽创面感染，为植皮创造条件。
用法用量
1.皮肤软组织细菌感染，每日患处涂药2次。|2.清创后，小面积烧伤可将本品直接涂在创面上，或将本品均匀地搓在无菌纱布上，将带药的纱布贴敷在创面上，创面可半暴露或包扎。
不良反应
主要为过敏反应，有皮疹、皮肤瘙痒，偶可发生渗出性多形性红斑及血管神经性水肿。一过性疼痛较少见。
禁忌
对本品及任何一种其他喹诺酮类药过敏者禁用。
注意事项
严重肾功能不全者慎用。
贮藏
避光，密封
规格
10g:0.1g。
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据。National Medical Products Administration (China) medicine-registration data.
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence.