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FENOFIBRATE RBX fenofibrate 48mg film coated tablets blister pack
Approved
STANDARD
FENOFIBRATE RBX fenofibrate 48mg film coated tablets blister pack
Sun Pharma ANZ Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
3cc4487ab53ef884
Company
Sun Pharma ANZ Pty Ltd
Type
Standard
Approval Details
Approval Id
3cc4487ab53ef884
Product Name
FENOFIBRATE RBX fenofibrate 48mg film coated tablets blister pack
Artg Id
233493
Artg Name
FENOFIBRATE RBX fenofibrate 48mg film coated tablets blister pack
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
Consumer Medicine Info
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2019-CMI-02248-1
Product Information
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-PI-01714-1
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
3cc4487ab53ef884
Type
Standard
Back to TGA Approvals
FENOFIBRATE RBX fenofibrate 48mg film coated tablets blister pack - TGA Drug Approval Details