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VITRAKVI larotrectinib (as sulfate) 25 mg hard capsule bottle - TGA Drug Approval Details
Approvals
/
TGA
/
VITRAKVI larotrectinib (as sulfate) 25 mg hard capsule bottle
Approved
STANDARD
VITRAKVI larotrectinib (as sulfate) 25 mg hard capsule bottle
Bayer Australia Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
1d64087f0d8973f3
Company
Bayer Australia Ltd
Type
Standard
Approval Details
Approval Id
1d64087f0d8973f3
Product Name
VITRAKVI larotrectinib (as sulfate) 25 mg hard capsule bottle
Artg Id
320237
Artg Name
VITRAKVI larotrectinib (as sulfate) 25 mg hard capsule bottle
Sponsor
Bayer Australia Ltd
Company Detail Path
/organization/bayer-australia-ltd
Artg Date
2020-09-07
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
REP
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/74e3eb8086e1935a5eeaa55dc9f05654.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/91c2ee80844939c64859343d93ff25a3.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
1d64087f0d8973f3
Type
Standard
Back to TGA Approvals