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ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack - TGA Drug Approval Details
Approvals
/
TGA
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ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack
Approved
STANDARD
ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
e680b93e045289e3
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
e680b93e045289e3
Product Name
ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack
Artg Id
332994
Artg Name
ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2021-02-22
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-CMI-01091-1
Product Information
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2023-PI-01090-1
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
e680b93e045289e3
Type
Standard
Back to TGA Approvals