Approvals/TGA/BISOLVON DRY dextromethorphan hydrobromide monohydrate 10.5 mg honey lime flavour pastille blister pack (reformulation)

Approved

STANDARD

BISOLVON DRY dextromethorphan hydrobromide monohydrate 10.5 mg honey lime flavour pastille blister pack (reformulation)

Approval Id: aa1a5096a6465f02
Product Name: BISOLVON DRY dextromethorphan hydrobromide monohydrate 10.5 mg honey lime flavour pastille blister pack (reformulation)
Artg Id: 460149
Artg Name: BISOLVON DRY dextromethorphan hydrobromide monohydrate 10.5 mg honey lime flavour pastille blister pack (reformulation)
Sponsor: Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path: /organization/sanofi-aventis-healthcare-pty-ltd
Artg Date: 2024-08-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/943d43c8137d2d68b51bf0ee14e15fee.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/af353947946776fb97c237750c804c0c.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

aa1a5096a6465f02

Type

Standard