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

Approved

STANDARD

METHYLPHENIDATE XR ARX methylphenidate hydrochloride 36 mg modified release tablet bottle

Teva Pharma Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 0568c831ce6e7fb7
Product Name: METHYLPHENIDATE XR ARX methylphenidate hydrochloride 36 mg modified release tablet bottle
Artg Id: 344277
Artg Name: METHYLPHENIDATE XR ARX 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: 2021-06-24
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/112f3718dca3df8e60361bf045565c3c.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/edd136adc353fb3b49fde2cca44daa7a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

0568c831ce6e7fb7

Type

Standard