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ACTILYSE alteplase (rch) 20mg powder for injection, vial with diluent vial - TGA Drug Approval Details
Approvals
/
TGA
/
ACTILYSE alteplase (rch) 20mg powder for injection, vial with diluent vial
Approved
STANDARD
ACTILYSE alteplase (rch) 20mg powder for injection, vial with diluent vial
Boehringer Ingelheim Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
097231c62e67f2b9
Company
Boehringer Ingelheim Pty Ltd
Type
Standard
Approval Details
Approval Id
097231c62e67f2b9
Product Name
ACTILYSE alteplase (rch) 20mg powder for injection, vial with diluent vial
Artg Id
43375
Artg Name
ACTILYSE alteplase (rch) 20 mg powder for injection vial with diluent vial
Sponsor
Boehringer Ingelheim Pty Ltd
Company Detail Path
/organization/boehringer-ingelheim-pty-ltd
Artg Date
1993-05-06
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Product Information
https://medical-cdn.nocode.com/drug_tga/a76086df442d92b70b55c1dd33bea61c.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
097231c62e67f2b9
Type
Standard
Back to TGA Approvals