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RITALIN 10 methylphenidate hydrochloride 10 mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
RITALIN 10 methylphenidate hydrochloride 10 mg tablet blister pack
Approved
STANDARD
RITALIN 10 methylphenidate hydrochloride 10 mg tablet blister pack
Novartis Pharmaceuticals Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
910e801f99947987
Company
Novartis Pharmaceuticals Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
910e801f99947987
Product Name
RITALIN 10 methylphenidate hydrochloride 10 mg tablet blister pack
Artg Id
11052
Artg Name
RITALIN 10 methylphenidate hydrochloride 10mg tablet blister pack
Sponsor
Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path
/organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date
1991-08-02
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/6a3a83d45e642d2e4349a91062e4a21d.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/9cf3052983492e663eece4e328cb5a6a.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
910e801f99947987
Type
Standard
Back to TGA Approvals
