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CUVITRU normal immunoglobulin (human) infusion 20% for subcutaneous use in glass vial
Approved
STANDARD
CUVITRU normal immunoglobulin (human) infusion 20% for subcutaneous use in glass vial
Takeda Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
79916fc8887f01c4
Company
Takeda Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
79916fc8887f01c4
Product Name
CUVITRU normal immunoglobulin (human) infusion 20% for subcutaneous use in glass vial
Artg Id
282579
Artg Name
CUVITRU normal immunoglobulin (human) infusion 20% for subcutaneous use in glass vial
Sponsor
Takeda Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/takeda-pharmaceuticals-australia-pty-ltd
Artg Date
2017-10-05
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/b71d50deffe938abd1276266208eed2f.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/959c2f356dbf2668b1a6b6d3ae935a2d.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
79916fc8887f01c4
Type
Standard
Back to TGA Approvals
CUVITRU normal immunoglobulin (human) infusion 20% for subcutaneous use in glass vial - TGA Drug Approval Details