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ELIGARD leuprorelin acetate 22.5mg modified release injection syringe - TGA Drug Approval Details
Approvals
/
TGA
/
ELIGARD leuprorelin acetate 22.5mg modified release injection syringe
Approved
STANDARD
ELIGARD leuprorelin acetate 22.5mg modified release injection syringe
Mundipharma Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
240bab304b3b9927
Company
Mundipharma Pty Ltd
Type
Standard
Approval Details
Approval Id
240bab304b3b9927
Product Name
ELIGARD leuprorelin acetate 22.5mg modified release injection syringe
Artg Id
97450
Artg Name
ELIGARD leuprorelin acetate 22.5mg modified release injection syringe
Sponsor
Mundipharma Pty Ltd
Company Detail Path
/organization/mundipharma-pty-ltd
Artg Date
2003-11-26
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/7ef7f076e8884cef69ee7566d2753c01.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/fea015c2e822e8205f64d3d17e6d174e.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
240bab304b3b9927
Type
Standard
Back to TGA Approvals