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STREPSILS DRY COUGH LOZENGES dextromethorphan hydrobromide monohydrate 5mg blister pack - TGA Drug Approval Details
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 Date
Dec 9, 2025
Approval ID
73ebef5057fbf7cc
Company
Reckitt Benckiser Pty Ltd
Type
Standard
Approval Details
Approval Id
73ebef5057fbf7cc
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
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
73ebef5057fbf7cc
Type
Standard
Back to TGA Approvals
