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FENOFIBRATE RBX fenofibrate 48mg film coated tablets bottle - TGA Drug Approval Details
Approvals
/
TGA
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FENOFIBRATE RBX fenofibrate 48mg film coated tablets bottle
Approved
STANDARD
FENOFIBRATE RBX fenofibrate 48mg film coated tablets bottle
Sun Pharma ANZ Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
427acae54c8e559c
Company
Sun Pharma ANZ Pty Ltd
Type
Standard
Approval Details
Approval Id
427acae54c8e559c
Product Name
FENOFIBRATE RBX fenofibrate 48mg film coated tablets bottle
Artg Id
233489
Artg Name
FENOFIBRATE RBX fenofibrate 48mg film coated tablets bottle
Sponsor
Sun Pharma ANZ Pty Ltd
Company Detail Path
/organization/sun-pharma-anz-pty-ltd
Artg Date
2016-02-29
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
427acae54c8e559c
Type
Standard
Back to TGA Approvals
