Approvals/TGA/BISOLVON CHESTY FORTE bromhexine hydrochloride 8mg tablet blister pack

Approved

STANDARD

BISOLVON CHESTY FORTE bromhexine hydrochloride 8mg tablet blister pack

Approval Id: 25ed2a79383992fc
Product Name: BISOLVON CHESTY FORTE bromhexine hydrochloride 8mg tablet blister pack
Artg Id: 125375
Artg Name: BISOLVON CHESTY FORTE bromhexine hydrochloride 8mg tablet blister pack
Sponsor: Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare
Company Detail Path: /organization/sanofi-aventis-healthcare-pty-ltd
Artg Date: 2006-01-25
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-CMI-01390-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2021-PI-01391-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

25ed2a79383992fc

Type

Standard