Recorded Chinese product: 乌头注射液乌头注射液
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
- 修正药业集团长春高新制药有限公司Chinese legal name: 修正药业集团长春高新制药有限公司
主要成分Active Ingredients
- 生川乌Shengchuan Wu
- 生草乌Shengcao Wu
药物知识说明
生川乌是一种在国家药监局注册认定的药品。该药品含有生川乌、生草乌-2e413eb6等成分。
该药品关联的活性成分包括:生川乌Shengchuan Wu、生草乌Shengcao Wu。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:修正药业集团长春高新制药有限公司Chinese legal name: 修正药业集团长春高新制药有限公司。
您可以探索含有相同成分的其他药品:生川乌-cb962a36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: 乌头注射液) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 生川乌Shengchuan Wu, 生草乌Shengcao Wu.
Manufacturers recorded for this product: 修正药业集团长春高新制药有限公司Chinese legal name: 修正药业集团长春高新制药有限公司.
Explore other medicines containing the same ingredient: 生川乌 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: 乌头注射液Recorded Chinese product: 乌头注射液
- 剂型Dosage form: 注射剂Injection
- 规格Specification: 1ml:0.62mg(乌头原碱)Recorded Chinese specification: 1ml:0.62mg(乌头原碱)
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
- 修正药业集团长春高新制药有限公司Chinese legal name: 修正药业集团长春高新制药有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字Z22025038
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Z22025038
Manufacturer
Chinese legal name: 修正药业集团长春高新制药有限公司
Traditional functions
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
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Z22025038
生产企业
修正药业集团长春高新制药有限公司
功能主治
镇静,止痛。用于胃癌、肝癌等晚期癌症的疼痛。
用法用量
肌内注射,一次1~2ml,一日1~2次。
不良反应
偶见白细胞下降,停药后即自行恢复。
禁忌
尚不明确。
注意事项
1.给药后如出现口干、头晕、恶心等不适者,应减量或停药。|2.偶见白细胞下降,停药后即自行恢复。|3.本品应在医生指导下用药,严格控制剂量。
贮藏
密闭保存。
规格
1ml:0.62mg(乌头原碱)
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.