GMPc Vietnam JSC
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Bộ Y tế yêu cầu rút nguyên liệu salbutamol trong 9 loại thuốc

05/10/2016 | 976 | Tin tức Tổng hợp

Cục trưởng Cục Quản lý Dược (Bộ Y tế) Trương Quốc Cường cho hay, đơn vị này vừa có có công văn số 19197/QLD-ĐK về việc rút nguyên liệu salbutamol trong 9 loại thuốc ra khỏi Danh mục nguyên liệu hoạt chất làm thuốc được phép nhập khẩu không yêu cầu có giấy phép nhập khẩu của các thuốc trong nước đã được cấp số đăng ký.
 
 
Cục Quản lý dược đã thông báo tới các công ty đăng ký, sản xuất thuốc trong nước về việc rút nguyên liệu salbutamol trong 9 loại thuốc có sử dụng dược chất này.
 
Đó là các loại thuốc: Solmux Brocho (số đăng ký:VD-21576); Zensalbu nebules 2.5 và 5.0 (VD- 21553 và 2554); GP- Salbutamol hàm lượng 2,5mg/5ml, 5mg/5ml và 1mg/2ml (VD – 21690; 21691; 21905); Haslbu (VD- 22033); Salbutamol 2mg (VD- 23028); Salbucare (VD-22973). 
 
Các thuốc trên do Công ty Trách nhiệm hữu hạn United Internationa Pharma; Công ty Cổ phần dược phẩm CPC1 Hà Nội; Công ty Cổ phần dược phẩm Trung ương 2. Công ty TNHH MTV DP DHG… sản xuất. 
 
Theo Cục Quản lý Dược, salbutamol (loại thuốc có tác dụng làm giãn phế quản thường được dùng trong những trường hợp bệnh hô hấp có kèm theo co thắt phế quản) vốn là hoạt chất sử dụng làm thuốc điều trị cho người từ nhiều năm nay. 
 
Các thuốc thành phẩm chứa chất Salbutamol được sử dụng trong ngành y tế chủ yếu trong khoa hô hấp với các chỉ định thăm dò chức năng hô hấp, điều trị cơn hen, ngăn cơn co thắt phế quản do gắng sức, điều trị cơn hen nặng, viêm phế quản mạn tính, giãn phế nang./.

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  • GMPc Vietnam JSC
  • Head Office: No. 18, Mang Cam 1 Street, An Lac Green Symphony, Van Canh Ward, Hoai Duc District, Hanoi City
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  • Home
  • About Us
    • Summary information
    • Key Personnel
  • Services
    • WHO GMP Pharmaceutical facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • EU GMP Pharmaceutical Factory
      • Feasibility study report
      • Design detailed construction drawings
      • QM documentation – Validation
      • GMP application and product dossier application
      • Project management - Construction supervision
    • CGMP, ISO 22716-certified cosmetics facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • CGMP ASEAN Training and Guidance
      • Preparation of CGMP ASEAN/ ISO 22716 registration dossier
      • CGMP ASEAN Re-evaluation consultation
    • Health-supplement facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • HS GMP Training and Guidance
      • Preparation HS GMP registration dossier
      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing
      • Overall consultation
      • Detail Construction and MEP drawing
      • Designing, Constructing, Ensured Certification
      • Preparation of Registration Dossier
    • Pharmaceutical distribution center
      • Feasibility Study
      • Design and Information Technology Solutions
      • Project Management and Supervision
      • GSP registration and operation consultancy
    • GSP warehouses
      • Project feasibility study
      • Detail Construction and MEP drawing
      • GSP Training and Guidance
      • Overall Consultation on Designing And Constructing
      • GSP Re-evaluation consultation
    • Veterinary Pharmaceutical Facilities
      • Project Feasibility Study
      • Technology and Equipment consultation
      • Detail Construction and MEP Drawing
      • Project management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • GMP, GLP, GSP training
      • Basis knowledge
      • Intensive Training
    • Other GPs’s consultation
      • GLP inspection laboratories
      • GDP distribution systems
      • GPP pharmacy
      • WHO GACP medicinal materials
    • Register and Announce
      • Announcement of Imported Cosmetic
    • Dairy Factory
      • Overall Planning
      • Detailed Construction & MEP Design - Project Budgeting
      • Contractor/Supplier Consultation and Project Management
      • Training, Drafting registration dossier
  • Project
  • Video
  • GMP-Handbook
  • Faqs
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  • Contact
 
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