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METHYLPHENIDATE XR ARX methylphenidate hydrochloride18 mg modified release tablet bottle - TGA Drug Approval Details
Approvals
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TGA
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METHYLPHENIDATE XR ARX methylphenidate hydrochloride18 mg modified release tablet bottle
Approved
STANDARD
METHYLPHENIDATE XR ARX methylphenidate hydrochloride18 mg modified release tablet bottle
Teva Pharma Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
7d91c064749ef4ac
Company
Teva Pharma Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
7d91c064749ef4ac
Product Name
METHYLPHENIDATE XR ARX methylphenidate hydrochloride18 mg modified release tablet bottle
Artg Id
344274
Artg Name
METHYLPHENIDATE XR ARX methylphenidate hydrochloride18 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
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
7d91c064749ef4ac
Type
Standard
Back to TGA Approvals