Recorded Chinese product: 盐酸甲氯芬酯分散片盐酸甲氯芬酯分散片

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

主要成分Active Ingredients

药物知识说明

甲氯芬酯是一种在国家药监局注册认定的药品。该药品含有甲氯芬酯-8d6b35bd等成分。

该药品关联的活性成分包括:甲氯芬酯Jialv Fenzhi。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:湖南华纳大药厂有限公司Chinese legal name: 湖南华纳大药厂有限公司。

您可以探索含有相同成分的其他药品:甲氯芬酯-8d6b35bd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: 盐酸甲氯芬酯分散片) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 甲氯芬酯Jialv Fenzhi.

Manufacturers recorded for this product: 湖南华纳大药厂有限公司Chinese legal name: 湖南华纳大药厂有限公司.

Explore other medicines containing the same ingredient: 甲氯芬酯 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: 盐酸甲氯芬酯分散片Recorded Chinese product: 盐酸甲氯芬酯分散片
  • 剂型Dosage form: 片剂Tablets
  • 规格Specification: 0.1g0.1 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

  • 湖南华纳大药厂有限公司Chinese legal name: 湖南华纳大药厂有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H20080768

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H20080768

Manufacturer

Chinese legal name: 湖南华纳大药厂有限公司 (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

Protect from light and keep tightly closed.

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H20080768

生产企业

湖南华纳大药厂有限公司(国产)

适应症

外伤性昏迷、酒精中毒、新生儿缺氧症、儿童遗尿症。

用法用量

本品可加水分散后口服,也可将分散片含于口中吮服或吞服。成人:一次0.1~0.2g,一日3次,至少服用1周。儿童:一次0.1g,一日3次,至少服用1周。

不良反应

胃部不适、兴奋、失眠、倦怠、头痛。

禁忌

精神过度兴奋、锥体外系症状患者及对本品过敏者。

注意事项

高血压患者慎用。

贮藏

遮光,密封保存。

规格

0.1g

证据Evidence

  • 批准文号: 国药准字H20080768
  • rights: 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。

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.