Approvals/TGA/FEXOFENADINE-DRLA fexofenadine hydrochloride 180 mg film coated tablet blister pack

Approved

STANDARD

FEXOFENADINE-DRLA fexofenadine hydrochloride 180 mg film coated tablet blister pack

Dr Reddys Laboratories Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 5c717324e3efb4a0
Product Name: FEXOFENADINE-DRLA fexofenadine hydrochloride 180 mg film coated tablet blister pack
Artg Id: 182787
Artg Name: FEXOFENADINE-DRLA fexofenadine hydrochloride 180 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

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

5c717324e3efb4a0

Type

Standard