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盐酸呋喃硫胺Fursultiamine Hydrochloride
盐酸呋喃硫胺Fursultiamine Hydrochloride
盐酸呋喃硫胺Fursultiamine Hydrochloride

盐酸呋喃硫胺Fursultiamine Hydrochloride

更新时间:2025-06-05

价格:
CAS号: 2105-43-3
药典: 中国药典,美国药典,英国药典,欧洲药典,日本药典,企业标准
级别: 药用级、食品级
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产品名称: 盐酸呋喃硫胺Fursultiamine Hydrochloride
产品分类: 维生素类
CAS号: 2105-43-3
药典: 中国药典,美国药典,英国药典,欧洲药典,日本药典,企业标准
级别: 药用级、食品级
产品关键词: Fursultiamine Hydrochloride,盐酸呋喃硫胺,维生素B1
是否为生产商:
主要销售市场: 中国,北美洲,中/南美洲,西欧,东欧,大洋洲,亚洲,中东,非洲
是否提供样品:

产品描述:

盐酸呋喃硫胺 Fursultiamine Hydrochloride

产品简介 / Product Overview:
盐酸呋喃硫胺是一种高效的维生素B1衍生物,主要用于神经系统疾病、慢性疲劳综合征以及B族维生素缺乏的相关治疗领域。我们可稳定供应高纯度、符合国际药典标准的盐酸呋喃硫胺原料药。
Fursultiamine Hydrochloride is an effective derivative of vitamin B1, widely used for neurological disorders, chronic fatigue syndrome, and vitamin B complex deficiency treatments. We provide stable supply of high-purity API compliant with major international pharmacopeias.



质量控制 / Quality Control:
我们严格按照中国GMP及ICH Q7标准进行生产,建立了完善的质量体系,确保每一批产品的质量安全、稳定、可追溯。
Produced under China GMP and ICH Q7 guidelines, our product undergoes rigorous quality control to ensure safety, stability, and full traceability.

  • 多项检测方法:HPLC、IR、UV、干燥失重、残留溶剂等全面控制Multiple analytical methods: HPLC, IR, UV, LOD, residual solvents, etc.
  • 产品符合EP/USP/JP等多国药典标准Fully compliant with EP/USP/JP and other pharmacopoeial standards
  • 提供稳定性研究、杂质谱分析、批记录、工艺验证资料Stability data, impurity profile, batch records and process validation available


供货能力 / Supply Capability:
我们拥有独立的中试与商业化生产车间,年产能力充足,常年备有现货,可快速响应全球客户的订单需求。
With dedicated pilot and commercial-scale production lines, we offer reliable annual capacity and ready stock to fulfill global orders quickly.

  • 年产能充足,支持批量定制与分装需求Sufficient annual capacity with custom packing options
  • 提供样品,COA,MSDS,注册支持文件(如DMF)Samples, COA, MSDS, and registration-supporting documents (e.g. DMF) available
  • 支持客户注册、技术问答与现场审计Registration assistance, technical Q&A, and on-site audits supported


国际适配 / Global Compliance:
我们的产品已通过多国客户审计,可满足全球多个地区的注册与质量要求。
Our API has been audited by clients from multiple countries and is compatible with registration and regulatory standards worldwide.

  • 日本市场:符合JP药典,多家日本客户稳定采购Japan: JP compliant, audited and regularly purchased by Japanese clients
  • 欧盟市场:支持CTD资料,适配EU DMF系统EU: CTD dossier available, adaptable to EU DMF system
  • 中国市场:按NMPA要求备案,支持一致性评价使用China: Filed with NMPA, suitable for consistency evaluation
  • 其他地区:可定制标准,快速配合客户注册需求Other markets: Standard customization and fast registration support available


联系我们 / Contact Us:

caoxin@hnxspharma.com

+8618395288756

如需样品、报价或技术资料,请与我们销售团队联系,我们将竭诚为您服务。
For samples, quotations, or technical documents, please contact our sales team — we are ready to support your business.


公司简介

湖南先施制药有限公司成立于2021年5月,位于湖南浏阳经济技术开发区北区,占地面积85亩,一期建筑面积40000㎡;公司现已建成原料药生产车间,固体制剂、小容量注射剂、软胶囊、口服溶液、大输液、软膏制剂车间;公司配套2000㎡分析检验中心,3200㎡研发实验室,日污水处理能力超450吨的污水处理系统。
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盐酸呋喃硫胺 Fursultiamine Hydrochloride产品简介 / Product Overview:盐酸呋喃硫胺是一种高效的维生素B1衍生物,主要用于神经系统疾病、慢性疲劳综合征以及B族维生素缺乏的相关治疗领域。我们可稳定供应高纯度、符合国际药典标准的盐酸呋喃硫胺原料药。Fursultiamine Hydrochloride is an effective derivative of vitamin B1, widely used for neurological disorders, chronic fatigue syndrome, and vitamin B complex deficiency treatments. We provide stable supply of high-purity API compliant with major international pharmacopeias.质量控制 / Quality Control:我们严格按照中国GMP及ICH Q7标准进行生产,建立了完善的质量体系,确保每一批产品的质量安全、稳定、可追溯。Produced under China GMP and ICH Q7 guidelines, our product undergoes rigorous quality control to ensure safety, stability, and full traceability.多项检测方法:HPLC、IR、UV、干燥失重、残留溶剂等全面控制Multiple analytical methods: HPLC, IR, UV, LOD, residual solvents, etc.产品符合EP/USP/JP等多国药典标准Fully compliant with EP/USP/JP and other pharmacopoeial standards提供稳定性研究、杂质谱分析、批记录、工艺验证资料Stability data, impurity profile, batch records and process validation available供货能力 / Supply Capability:我们拥有独立的中试与商业化生产车间,年产能力充足,常年备有现货,可快速响应全球客户的订单需求。With dedicated pilot and commercial-scale production lines, we offer reliable annual capacity and ready stock to fulfill global orders quickly.年产能充足,支持批量定制与分装需求Sufficient annual capacity with custom packing options提供样品,COA,MSDS,注册支持文件(如DMF)Samples, COA, MSDS, and registration-supporting documents (e.g. DMF) available支持客户注册、技术问答与现场审计Registration assistance, technical Q&A, and on-site audits supported国际适配 / Global Compliance:我们的产品已通过多国客户审计,可满足全球多个地区的注册与质量要求。Our API has been audited by clients from multiple countries and is compatible with registration and regulatory standards worldwide.日本市场:符合JP药典,多家日本客户稳定采购Japan: JP compliant, audited and regularly purchased by Japanese clients欧盟市场:支持CTD资料,适配EU DMF系统EU: CTD dossier available, adaptable to EU DMF system中国市场:按NMPA要求备案,支持一致性评价使用China: Filed with NMPA, suitable for consistency evaluation其他地区:可定制标准,快速配合客户注册需求Other markets: Standard customization and fast registration support available联系我们 / Contact Us:caoxin@hnxspharma.com+8618395288756如需样品、报价或技术资料,请与我们销售团队联系,我们将竭诚为您服务。For samples, quotations, or technical documents, please contact our sales team — we are ready to support your business.
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