Recorded Chinese product: 盐酸特拉唑嗪胶囊盐酸特拉唑嗪胶囊
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
- 世贸天阶制药(江苏)有限责任公司Chinese legal name: 世贸天阶制药(江苏有限责任公司)
主要成分Active Ingredients
- 特拉唑嗪Tela Zuoqin
药物知识说明
特拉唑嗪是一种在国家药监局注册认定的药品。该药品含有特拉唑嗪-930826ef等成分。
该药品关联的活性成分包括：特拉唑嗪Tela Zuoqin。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：世贸天阶制药(江苏)有限责任公司Chinese legal name: 世贸天阶制药(江苏有限责任公司)。
您可以探索含有相同成分的其他药品：特拉唑嗪-930826ef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: 盐酸特拉唑嗪胶囊) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 特拉唑嗪Tela Zuoqin.
Manufacturers recorded for this product: 世贸天阶制药(江苏)有限责任公司Chinese legal name: 世贸天阶制药(江苏有限责任公司).
Explore other medicines containing the same ingredient: 特拉唑嗪 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: 盐酸特拉唑嗪胶囊Recorded Chinese product: 盐酸特拉唑嗪胶囊
- 剂型Dosage form: 片剂Tablets
- 规格Specification: 2mg*12片2 mg × 12 tablets
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
- 世贸天阶制药(江苏)有限责任公司Chinese legal name: 世贸天阶制药(江苏有限责任公司)
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H19990108
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H19990108
Manufacturer
Chinese legal name: 世贸天阶制药(江苏)有限责任公司 (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
2 mg × 12 tablets
中文说明书原文Original Chinese source label
批准文号
国药准字H19990108
生产企业
世贸天阶制药(江苏)有限责任公司(国产)
适应症
用于治疗高血压，可单独应用或与其它抗高血压药同时使用。用于改善良性前列腺增生症患者的排尿症状。如：尿频、尿急、尿线变细、排尿困难、夜尿增多、排尿不尽感等。
用法用量
口服。一日一次，首次睡前服用。开始剂量1mg，停药后需重新开始治疗者，亦必须从1mg开始渐增剂量。 高血压：常用剂量为一日1～10mg，最大剂量为一日20mg。剂量逐渐增加直到出现满意的疗效。 良性前列腺增生：一日一次，每次2mg，每晚睡前服用。
不良反应
本品主要不良反应有：头痛、头晕、无力、心悸、恶心、体位性低血压等。这些反应通常轻微，继续治疗多可自行消失，必要时可减量。
禁忌
对本品过敏者禁用。
注意事项
孕妇及哺乳期妇女慎用，病人在开始及增加剂量时应避免可导致头晕或乏力的突然性姿势变化或行动。
贮藏
遮光，密封保存。
规格
2mg*12片
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.