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MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2) - TGA Drug Approval Details
Approvals
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TGA
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MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2)
Approved
STANDARD
MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2)
Johnson & Johnson Pacific Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
3a1a3f11ae19e46e
Company
Johnson & Johnson Pacific Pty Ltd
Type
Standard
Approval Details
Approval Id
3a1a3f11ae19e46e
Product Name
MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2)
Artg Id
126090
Artg Name
MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2)
Sponsor
Johnson & Johnson Pacific Pty Ltd
Company Detail Path
/organization/johnson-and-johnson-pacific-pty-ltd
Artg Date
2006-03-10
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
3a1a3f11ae19e46e
Type
Standard
Back to TGA Approvals
