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SOMAVERT pegvisomant (rbe) 20mg powder for injection vial and diluent in pre-filled syringe
Approved
STANDARD
SOMAVERT pegvisomant (rbe) 20mg powder for injection vial and diluent in pre-filled syringe
Pfizer Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
9267d542af827356
Company
Pfizer Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
9267d542af827356
Product Name
SOMAVERT pegvisomant (rbe) 20mg powder for injection vial and diluent in pre-filled syringe
Artg Id
286630
Artg Name
SOMAVERT pegvisomant (rbe) 20mg powder for injection vial and diluent in pre-filled syringe
Sponsor
Pfizer Australia Pty Ltd
Company Detail Path
/organization/pfizer-australia-pty-ltd
Artg Date
2017-05-31
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/1ada0ddb3eb6db94fbfa570ece6a1e91.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/38caad8dff2d69777da521a10b02a14f.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
9267d542af827356
Type
Standard
Back to TGA Approvals
SOMAVERT pegvisomant (rbe) 20mg powder for injection vial and diluent in pre-filled syringe - TGA Drug Approval Details