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TELFAST fexofenadine hydrochloride 120mg tablet blister pack
Approved
STANDARD
TELFAST fexofenadine hydrochloride 120mg tablet blister pack
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
42c9534f785f6884
Company
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Type
Standard
Approval Details
Approval Id
42c9534f785f6884
Product Name
TELFAST fexofenadine hydrochloride 120mg tablet blister pack
Artg Id
63339
Artg Name
TELFAST fexofenadine hydrochloride 120mg tablet blister pack
Sponsor
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path
/organization/sanofi-aventis-healthcare-pty-ltd
Artg Date
1998-03-30
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/a98509135f42d916537152fb23594984.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/b852067bb5fb02b18dcf5b097421f32e.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
42c9534f785f6884
Type
Standard
Back to TGA Approvals
TELFAST fexofenadine hydrochloride 120mg tablet blister pack - TGA Drug Approval Details
