Approvals/TGA/RITALIN LA methylphenidate hydrochloride 10 mg modified-release capsule bottle

Approved

STANDARD

RITALIN LA methylphenidate hydrochloride 10 mg modified-release capsule bottle

Approval Id: 6c0167d9f65ddd44
Product Name: RITALIN LA methylphenidate hydrochloride 10 mg modified-release capsule bottle
Artg Id: 160228
Artg Name: RITALIN LA methylphenidate hydrochloride 10 mg modified release capsule bottle
Sponsor: Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path: /organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date: 2009-12-18
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-2010-CMI-05347-3
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-03175-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

6c0167d9f65ddd44

Type

Standard