Approvals/TGA/PRODEINE paracetamol 500 mg and codeine phosphate hemihydrate 9.6 mg tablet blister pack

Approved

STANDARD

PRODEINE paracetamol 500 mg and codeine phosphate hemihydrate 9.6 mg tablet blister pack

Sanofi-Aventis Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 5ec68a1b539ec5fb
Product Name: PRODEINE paracetamol 500 mg and codeine phosphate hemihydrate 9.6 mg tablet blister pack
Artg Id: 200605
Artg Name: PRODEINE paracetamol 500 mg and codeine phosphate hemihydrate 9.6 mg tablet blister pack
Sponsor: Sanofi-Aventis Australia Pty Ltd
Company Detail Path: /organization/sanofi-aventis-australia-pty-ltd
Artg Date: 2012-09-04
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/191dba6ec30f2b23a0df04af6e95a908.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/c0ea5abf26dd30b505c00fe2be3e5860.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

5ec68a1b539ec5fb

Type

Standard