Ondansetron Hydrochloride Injection (盐酸昂丹司琼注射液)盐酸昂丹司琼注射液

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

主要成分Active Ingredients

药物知识说明

昂丹司琼是一种在国家药监局注册认定的药品。该药品含有昂丹司琼-6ddb88c1等成分。

该药品关联的活性成分包括:昂丹司琼ondansetron。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:济南永宁制药股份有限公司Chinese legal name: 济南永宁制药股份有限公司。

您可以探索含有相同成分的其他药品:昂丹司琼-6ddb88c1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

ondansetron is a medicine registered with the national drug regulatory authority. It contains ondansetron as active ingredient(s).

Active ingredients associated with this product: ondansetronondansetron.

Manufacturers recorded for this product: 济南永宁制药股份有限公司Chinese legal name: 济南永宁制药股份有限公司.

Explore other medicines containing the same ingredient: ondansetron products.

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: 盐酸昂丹司琼注射液Ondansetron Hydrochloride Injection (盐酸昂丹司琼注射液)
  • 剂型Dosage form: 注射剂Injection
  • 规格Specification: 4m1:8mg(按昂丹司琼计算)Recorded Chinese description: 4m1:8mg(按昂丹司琼计算)

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

  • 济南永宁制药股份有限公司Chinese legal name: 济南永宁制药股份有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H20064864

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H20064864

Manufacturer

Chinese legal name: 济南永宁制药股份有限公司 (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.

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H20064864

生产企业

济南永宁制药股份有限公司(国产)

适应症

止吐药。用于: ①细胞毒性药物化疗和放射治疗引起的恶心呕吐; ②预防和治疗手术后的恶性呕吐。

用法用量

本品可通过静脉和肌内注射给药,给药剂量和途径应视呕吐严重程度而定。 成人剂量一般每天8mg。 1.对于高度催吐的化疗药引起的呕吐在化疗前30分钟,化疗后4小时、8小时各静脉滴注本品8mg,停止化疗以后每8―12小时口服片剂8mg。 2.对催吐程度不太强的化疗药引起的呕吐,化疗前30分钟静脉注本品8mg,以后每8―12小时口服片剂8mg,连用5天。 3.对于放射治疗引起的呕吐,首剂应于放疗前1―2小时口服片剂8mg,以后每8小时口服8mg。 4.对于预防和治疗手术后呕吐,成人可于麻醉诱导同时静脉滴注本品4mg,对已出现术后恶心呕吐时,可缓慢静脉滴注本品4mg进行治疗。输注时间应不小于15分钟。

不良反应

可有头痛,头部和上腹部有温热感,腹部不适、便秘、口干、皮疹、注射部位局部反应,偶见支气管哮喘或过敏反应,暂时性无症状转氨酶升高。上述反应一般轻微,不需特殊处理。偶见运动失调,癫痫发作,胸痛、心律不齐、低血压及心动过缓等罕见报告。

禁忌

对本品过敏者禁用。胃肠梗阻者禁用。

贮藏

遮光,密闭,在阴凉处(不超过20℃)保存。

规格

4m1:8mg(按昂丹司琼计算)

证据Evidence

  • 批准文号: 国药准字H20064864
  • 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.