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TELFAST ORAL LIQUID fexofenadine hydrochloride 6 mg/mL oral suspension bottle
Approved
STANDARD
TELFAST ORAL LIQUID fexofenadine hydrochloride 6 mg/mL oral suspension bottle
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
37547a48170189c4
Company
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Type
Standard
Approval Details
Approval Id
37547a48170189c4
Product Name
TELFAST ORAL LIQUID fexofenadine hydrochloride 6 mg/mL oral suspension bottle
Artg Id
156262
Artg Name
TELFAST ORAL LIQUID fexofenadine hydrochloride 6 mg/mL oral suspension bottle
Sponsor
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path
/organization/sanofi-aventis-healthcare-pty-ltd
Artg Date
2008-10-28
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/1be3d27447458c1daf26b0eef9af246a.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/b852067bb5fb02b18dcf5b097421f32e.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
37547a48170189c4
Type
Standard
Back to TGA Approvals
TELFAST ORAL LIQUID fexofenadine hydrochloride 6 mg/mL oral suspension bottle - TGA Drug Approval Details