Approvals/TGA/RITALIN LA methylphenidate hydrochloride 40mg modified release capsule bottle (NF)

Approved

STANDARD

RITALIN LA methylphenidate hydrochloride 40mg modified release capsule bottle (NF)

Approval Id: be0f1a09e3470509
Product Name: RITALIN LA methylphenidate hydrochloride 40mg modified release capsule bottle (NF)
Artg Id: 82959
Artg Name: RITALIN LA methylphenidate hydrochloride 40mg modified release capsule bottle
Sponsor: Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path: /organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date: 2002-08-21
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/7ed06b114826466d7a7f244ef27e0258.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/9cf3052983492e663eece4e328cb5a6a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

be0f1a09e3470509

Type

Standard