Approvals/TGA/BENADRYL DRY IRRITATING COUGH FORTE dextromethorphan hydrobromide monohydrate 3 mg/mL oral liquid bottle

Approved

STANDARD

BENADRYL DRY IRRITATING COUGH FORTE dextromethorphan hydrobromide monohydrate 3 mg/mL oral liquid bottle

Johnson & Johnson Pacific Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 4f5fdc42e5411464
Product Name: BENADRYL DRY IRRITATING COUGH FORTE dextromethorphan hydrobromide monohydrate 3 mg/mL oral liquid bottle
Artg Id: 473728
Artg Name: BENADRYL DRY IRRITATING COUGH FORTE dextromethorphan hydrobromide monohydrate 3 mg/mL oral liquid bottle
Sponsor: Johnson & Johnson Pacific Pty Ltd
Company Detail Path: /organization/johnson-and-johnson-pacific-pty-ltd
Artg Date: 2024-12-18
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

4f5fdc42e5411464

Type

Standard