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TRILEPTAL oxcarbazepine 600mg tablet film coated blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
TRILEPTAL oxcarbazepine 600mg tablet film coated blister pack
Approved
STANDARD
TRILEPTAL oxcarbazepine 600mg tablet film coated blister pack
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
3b07051e10ab57ff
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
3b07051e10ab57ff
Product Name
TRILEPTAL oxcarbazepine 600mg tablet film coated blister pack
Artg Id
76202
Artg Name
TRILEPTAL oxcarbazepine 600mg tablet film coated blister pack
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
2000-10-13
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/305111795e64471f027f9c1b3d669ddf.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/49534bc9e032e4ae97d0b4ceef253387.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
3b07051e10ab57ff
Type
Standard
Back to TGA Approvals
