Approvals/TGA/TEVETEN PLUS 600/12.5 eprosartan 600mg/hydrochlorothiazide 12.5mg tablet blister pack

Approved

STANDARD

TEVETEN PLUS 600/12.5 eprosartan 600mg/hydrochlorothiazide 12.5mg tablet blister pack

Viatris Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: faac12006fac1420
Product Name: TEVETEN PLUS 600/12.5 eprosartan 600mg/hydrochlorothiazide 12.5mg tablet blister pack
Artg Id: 143172
Artg Name: TEVETEN PLUS 600/12.5 eprosartan 600mg/hydrochlorothiazide 12.5mg tablet blister pack
Sponsor: Viatris Pty Ltd
Company Detail Path: /organization/viatris-pty-ltd
Artg Date: 2007-08-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/b12697133ba8e97c4acc06665e385a4f.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/7cae9947860933135036f0834b37dad0.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

faac12006fac1420

Type

Standard