Approvals/TGA/STREPSILS DRY COUGH LOZENGES dextromethorphan hydrobromide monohydrate 5mg blister pack

Approved

STANDARD

STREPSILS DRY COUGH LOZENGES dextromethorphan hydrobromide monohydrate 5mg blister pack

Reckitt Benckiser Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 89b105fbd8f803a6
Product Name: STREPSILS DRY COUGH LOZENGES dextromethorphan hydrobromide monohydrate 5mg blister pack
Artg Id: 69834
Artg Name: STREPSILS DRY COUGH LOZENGES dextromethorphan hydrobromide monohydrate 5mg blister pack
Sponsor: Reckitt Benckiser Pty Ltd
Company Detail Path: /organization/reckitt-benckiser-australia-pty-ltd
Artg Date: 1999-07-09
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

89b105fbd8f803a6

Type

Standard