Approvals/TGA/METHYLPHENIDATE-TEVA XR methylphenidate hydrochloride 36 mg modified release tablet bottle

Approved

STANDARD

METHYLPHENIDATE-TEVA XR methylphenidate hydrochloride 36 mg modified release tablet bottle

Teva Pharma Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 6c28eb8a214a678d
Product Name: METHYLPHENIDATE-TEVA XR methylphenidate hydrochloride 36 mg modified release tablet bottle
Artg Id: 370900
Artg Name: METHYLPHENIDATE-TEVA XR methylphenidate hydrochloride 36 mg modified release tablet bottle
Sponsor: Teva Pharma Australia Pty Ltd
Company Detail Path: /organization/teva-pharma-australia-pty-ltd
Artg Date: 2021-10-13
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-2021-CMI-02435-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-PI-02263-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

6c28eb8a214a678d

Type

Standard