Approvals/TGA/Terbinafine-DRLA terbinafine (as hydrochloride) 250 mg tablet blister pack

Approved

STANDARD

Terbinafine-DRLA terbinafine (as hydrochloride) 250 mg tablet blister pack

Dr Reddys Laboratories Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f006bec65a338904
Product Name: Terbinafine-DRLA terbinafine (as hydrochloride) 250 mg tablet blister pack
Artg Id: 167575
Artg Name: Terbinafine-DRLA terbinafine (as hydrochloride) 250 mg tablet blister pack
Sponsor: Dr Reddys Laboratories Australia Pty Ltd
Company Detail Path: /organization/dr-reddys-laboratories-australia-pty-ltd
Artg Date: 2010-07-13
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2017-CMI-01521-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2011-PI-03199-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

f006bec65a338904

Type

Standard