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PANAMAX CO paracetamol 500 mg and codeine phosphate hemihydrate 8 mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
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PANAMAX CO paracetamol 500 mg and codeine phosphate hemihydrate 8 mg tablet blister pack
Approved
STANDARD
PANAMAX CO paracetamol 500 mg and codeine phosphate hemihydrate 8 mg tablet blister pack
Sanofi-Aventis Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
21f84b3a82be0b18
Company
Sanofi-Aventis Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
21f84b3a82be0b18
Product Name
PANAMAX CO paracetamol 500 mg and codeine phosphate hemihydrate 8 mg tablet blister pack
Artg Id
62661
Artg Name
PANAMAX CO paracetamol 500 mg and codeine phosphate hemihydrate 8 mg tablet blister pack
Sponsor
Sanofi-Aventis Australia Pty Ltd
Company Detail Path
/organization/sanofi-aventis-australia-pty-ltd
Artg Date
1997-12-15
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/5f82872475f2f033d48e9f4c74a386d7.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/8828e20bd8ea07cbf5018e31641898f0.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
21f84b3a82be0b18
Type
Standard
Back to TGA Approvals