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SOLU-CORTEF 100mg powder for injection vial - TGA Drug Approval Details
Approvals
/
TGA
/
SOLU-CORTEF 100mg powder for injection vial
Approved
STANDARD
SOLU-CORTEF 100mg powder for injection vial
Pfizer Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
1f3950bd9026cfb7
Company
Pfizer Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
1f3950bd9026cfb7
Product Name
SOLU-CORTEF 100mg powder for injection vial
Artg Id
12264
Artg Name
SOLU-CORTEF Hydrocortisone (as sodium succinate) 100mg Powder for Injection vial
Sponsor
Pfizer Australia Pty Ltd
Company Detail Path
/organization/pfizer-australia-pty-ltd
Artg Date
1991-08-02
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/c9be4b8b08432099b5e69434250d8a0d.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/dde7324578643d817e1e6b3be5281e91.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
1f3950bd9026cfb7
Type
Standard
Back to TGA Approvals