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SIMULECT basiliximab (rmc) 20mg powder for injection vial - TGA Drug Approval Details
Approvals
/
TGA
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SIMULECT basiliximab (rmc) 20mg powder for injection vial
Approved
STANDARD
SIMULECT basiliximab (rmc) 20mg powder for injection vial
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
97daf8e1ea95b911
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
97daf8e1ea95b911
Product Name
SIMULECT basiliximab (rmc) 20mg powder for injection vial
Artg Id
440470
Artg Name
SIMULECT basiliximab (rmc) 20mg powder for injection vial
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
2024-10-22
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Product Information
https://medical-cdn.nocode.com/drug_tga/564cad3a2e212fdfae77ece23f74d236.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
97daf8e1ea95b911
Type
Standard
Back to TGA Approvals
