Approvals/TGA/PRODEINEXTRA paracetamol 500mg & codeine phosphate hemihydrate 15mg film coated tablet blister pack

Approved

STANDARD

PRODEINEXTRA paracetamol 500mg & codeine phosphate hemihydrate 15mg film coated tablet blister pack

Sanofi-Aventis Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8547281f6828a449
Product Name: PRODEINEXTRA paracetamol 500mg & codeine phosphate hemihydrate 15mg film coated tablet blister pack
Artg Id: 205550
Artg Name: PRODEINEXTRA paracetamol 500mg & codeine phosphate hemihydrate 15mg film coated tablet blister pack
Sponsor: Sanofi-Aventis Australia Pty Ltd
Company Detail Path: /organization/sanofi-aventis-australia-pty-ltd
Artg Date: 2013-02-04
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/cf0b9e810c3a98295028c350bf7be9ce.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/1df70d10c51e3dcf5e5dc2137ed2586a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

8547281f6828a449

Type

Standard