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REPATHA evolocumab (rch) 140 mg/mL injection solution syringe - TGA Drug Approval Details
Approvals
/
TGA
/
REPATHA evolocumab (rch) 140 mg/mL injection solution syringe
Approved
STANDARD
REPATHA evolocumab (rch) 140 mg/mL injection solution syringe
Amgen Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
1ed84f2462830004
Company
Amgen Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
1ed84f2462830004
Product Name
REPATHA evolocumab (rch) 140 mg/mL injection solution syringe
Artg Id
231151
Artg Name
REPATHA evolocumab (rch) 140 mg/mL injection solution syringe
Sponsor
Amgen Australia Pty Ltd
Company Detail Path
/organization/amgen-australia-pty-ltd
Artg Date
2015-12-09
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Product Information
https://medical-cdn.nocode.com/drug_tga/de0e5ab92a5811514383dae8f0f63a34.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
1ed84f2462830004
Type
Standard
Back to TGA Approvals