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FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack
Approved
STANDARD
FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack
Dr Reddys Laboratories Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
f667f9506f5241db
Company
Dr Reddys Laboratories Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
f667f9506f5241db
Product Name
FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack
Artg Id
182786
Artg Name
FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack
Sponsor
Dr Reddys Laboratories Australia Pty Ltd
Company Detail Path
/organization/dr-reddys-laboratories-australia-pty-ltd
Artg Date
2011-05-02
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
f667f9506f5241db
Type
Standard
Back to TGA Approvals
FEXOFENADINE-DRLA fexofenadine hydrochloride 120 mg film coated tablet blister pack - TGA Drug Approval Details
