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BISOLVON DRY dextromethorphan hydrobromide monohydrate 2mg/mL oral liquid bottle
Approved
STANDARD
BISOLVON DRY dextromethorphan hydrobromide monohydrate 2mg/mL oral liquid bottle
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
d9be5ac5d6afd02d
Company
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Type
Standard
Approval Details
Approval Id
d9be5ac5d6afd02d
Product Name
BISOLVON DRY dextromethorphan hydrobromide monohydrate 2mg/mL oral liquid bottle
Artg Id
68185
Artg Name
BISOLVON DRY dextromethorphan hydrobromide monohydrate 2mg/mL oral liquid bottle
Sponsor
Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path
/organization/sanofi-aventis-healthcare-pty-ltd
Artg Date
1999-03-19
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/72df315a7056d3506c8cf602f86f3eb7.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/af353947946776fb97c237750c804c0c.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
d9be5ac5d6afd02d
Type
Standard
Back to TGA Approvals
BISOLVON DRY dextromethorphan hydrobromide monohydrate 2mg/mL oral liquid bottle - TGA Drug Approval Details
