Approvals/TGA/Olmesartan/HCT Sandoz 20/12.5 olmesartan medoxomil/hydrochlorothiazide 20/12.5 mg film-coated tablet blister pack

Approved

STANDARD

Olmesartan/HCT Sandoz 20/12.5 olmesartan medoxomil/hydrochlorothiazide 20/12.5 mg film-coated tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: d71aa0912f4e2866
Product Name: Olmesartan/HCT Sandoz 20/12.5 olmesartan medoxomil/hydrochlorothiazide 20/12.5 mg film-coated tablet blister pack
Artg Id: 221119
Artg Name: Olmesartan/HCT Sandoz 20/12.5 olmesartan medoxomil/hydrochlorothiazide 20/12.5 mg film-coated tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2015-02-05
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/543c9014e9347935a93efc7cb3087dcb.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/f9f3b11e0c8cacb25fcb5ba3ef55fbd7.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

d71aa0912f4e2866

Type

Standard