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BENADRYL MUCUS RELIEF guaifenesin 20 mg/mL oral liquid bottle - TGA Drug Approval Details
Approvals
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TGA
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BENADRYL MUCUS RELIEF guaifenesin 20 mg/mL oral liquid bottle
Approved
STANDARD
BENADRYL MUCUS RELIEF guaifenesin 20 mg/mL oral liquid bottle
Johnson & Johnson Pacific Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
a052fe8d7ea84917
Company
Johnson & Johnson Pacific Pty Ltd
Type
Standard
Approval Details
Approval Id
a052fe8d7ea84917
Product Name
BENADRYL MUCUS RELIEF guaifenesin 20 mg/mL oral liquid bottle
Artg Id
204233
Artg Name
BENADRYL MUCUS RELIEF guaifenesin 20 mg/mL oral liquid bottle
Sponsor
Johnson & Johnson Pacific Pty Ltd
Company Detail Path
/organization/johnson-and-johnson-pacific-pty-ltd
Artg Date
2012-12-19
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
a052fe8d7ea84917
Type
Standard
Back to TGA Approvals
