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SIMULECT basiliximab (rmc) 20mg powder for injection vial and diluent ampoule - TGA Drug Approval Details
Approvals
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TGA
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SIMULECT basiliximab (rmc) 20mg powder for injection vial and diluent ampoule
Approved
STANDARD
SIMULECT basiliximab (rmc) 20mg powder for injection vial and diluent ampoule
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 28, 2025
Approval ID
d45b0edd63d775c3
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
d45b0edd63d775c3
Product Name
SIMULECT basiliximab (rmc) 20mg powder for injection vial and diluent ampoule
Artg Id
66740
Artg Name
SIMULECT basiliximab (rmc) 20mg powder for injection vial and diluent ampoule
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
1999-02-18
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/363569833840542b775ec40b27ba615d.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/564cad3a2e212fdfae77ece23f74d236.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 28, 2025
Approval ID
d45b0edd63d775c3
Type
Standard
Back to TGA Approvals
