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TERRYWHITE CHEMMART IBUPROFEN 200 mg film-coated tablet blister pack (reformulation) - TGA Drug Approval Details
Approvals
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TGA
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TERRYWHITE CHEMMART IBUPROFEN 200 mg film-coated tablet blister pack (reformulation)
Approved
STANDARD
TERRYWHITE CHEMMART IBUPROFEN 200 mg film-coated tablet blister pack (reformulation)
NOUMED PHARMACEUTICALS PTY LTD
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
2d0110c610b50af0
Company
NOUMED PHARMACEUTICALS PTY LTD
Type
Standard
Approval Details
Approval Id
2d0110c610b50af0
Product Name
TERRYWHITE CHEMMART IBUPROFEN 200 mg film-coated tablet blister pack (reformulation)
Artg Id
361914
Artg Name
TERRYWHITE CHEMMART IBUPROFEN 200 mg film-coated tablet blister pack (reformulation)
Sponsor
NOUMED PHARMACEUTICALS PTY LTD
Company Detail Path
/organization/noumed-pharmaceuticals-pty-ltd
Artg Date
2021-04-14
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
2d0110c610b50af0
Type
Standard
Back to TGA Approvals