Approvals/TGA/VYALEV foslevodopa 2400 mg/10 mL and foscarbidopa 120 mg/10 mL solution for subcutaneous infusion vial

Approved

STANDARD

VYALEV foslevodopa 2400 mg/10 mL and foscarbidopa 120 mg/10 mL solution for subcutaneous infusion vial

AbbVie Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: dad7be3a4a54f0c3
Product Name: VYALEV foslevodopa 2400 mg/10 mL and foscarbidopa 120 mg/10 mL solution for subcutaneous infusion vial
Artg Id: 372902
Artg Name: VYALEV foslevodopa 2400 mg/10 mL and foscarbidopa 120 mg/10 mL solution for subcutaneous infusion vial
Sponsor: AbbVie Pty Ltd
Company Detail Path: /organization/abbvie-pty-ltd
Artg Date: 2024-03-27
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/386ba85a8d79de189dc87c1465bb0b26.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/82402bd4eac61eee85a2d507088c92d7.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

dad7be3a4a54f0c3

Type

Standard