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ELAPRASE idursulfase-rhu concentrate for solution for IV infusion vial - TGA Drug Approval Details
Approvals
/
TGA
/
ELAPRASE idursulfase-rhu concentrate for solution for IV infusion vial
Approved
STANDARD
ELAPRASE idursulfase-rhu concentrate for solution for IV infusion vial
Sanofi-Aventis Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
52703f9d39bfb04e
Company
Sanofi-Aventis Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
52703f9d39bfb04e
Product Name
ELAPRASE idursulfase-rhu concentrate for solution for IV infusion vial
Artg Id
129481
Artg Name
ELAPRASE idursulfase-rhu solution for IV infusion vial
Sponsor
Sanofi-Aventis Australia Pty Ltd
Company Detail Path
/organization/sanofi-aventis-australia-pty-ltd
Artg Date
2008-02-21
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/b41ed4531af21381c480bba60f633d45.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/38e1e16a023d95b553f18c933466f1a6.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
52703f9d39bfb04e
Type
Standard
Back to TGA Approvals