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ARTIGE methylphenidate hydrochloride 10mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
ARTIGE methylphenidate hydrochloride 10mg tablet blister pack
Approved
STANDARD
ARTIGE methylphenidate hydrochloride 10mg tablet blister pack
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
117f2cb33f9a864b
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
117f2cb33f9a864b
Product Name
ARTIGE methylphenidate hydrochloride 10mg tablet blister pack
Artg Id
117306
Artg Name
ARTIGE methylphenidate hydrochloride 10mg tablet blister pack
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
2005-06-02
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/4c4f321799ebae0bfc8f498150b6b0a1.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/2f62f1b23e488b6ad97aac1dd9e1a5fe.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 29, 2025
Approval ID
117f2cb33f9a864b
Type
Standard
Back to TGA Approvals
