Approvals/TGA/PRODEINE FORTE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack

Approved

STANDARD

PRODEINE FORTE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack

Sanofi-Aventis Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 1cfee9aafa297130
Product Name: PRODEINE FORTE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack
Artg Id: 93865
Artg Name: PRODEINE FORTE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack
Sponsor: Sanofi-Aventis Australia Pty Ltd
Company Detail Path: /organization/sanofi-aventis-australia-pty-ltd
Artg Date: 2003-04-28
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/c7c97722fe95d56fdca3ed31eef075bf.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/3a599700a21ae010e8872e09a06a3c8a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

1cfee9aafa297130

Type

Standard