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Hospira Deferoxamine Mesylate 500 mg Powder for Injection Vial - TGA Drug Approval Details
Approvals
/
TGA
/
Hospira Deferoxamine Mesylate 500 mg Powder for Injection Vial
Approved
STANDARD
Hospira Deferoxamine Mesylate 500 mg Powder for Injection Vial
Hospira Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
d2a00bb486921592
Company
Hospira Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
d2a00bb486921592
Product Name
Hospira Deferoxamine Mesylate 500 mg Powder for Injection Vial
Artg Id
378150
Artg Name
Hospira Deferoxamine Mesylate 500 mg Powder for Injection Vial
Sponsor
Hospira Australia Pty Ltd
Company Detail Path
/organization/hospira-australia-pty-ltd
Artg Date
2021-11-17
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
LIE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
d2a00bb486921592
Type
Standard
Back to TGA Approvals
