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PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH INFLAMMATION AND PAIN RELIEF ibuprofen sodium dihydrate 512 mg tablets blister pack - TGA Drug Approval Details
Approvals
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TGA
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PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH INFLAMMATION AND PAIN RELIEF ibuprofen sodium dihydrate 512 mg tablets blister pack
Approved
STANDARD
PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH INFLAMMATION AND PAIN RELIEF ibuprofen sodium dihydrate 512 mg tablets blister pack
NOUMED PHARMACEUTICALS PTY LTD
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
e1917a24715e3587
Company
NOUMED PHARMACEUTICALS PTY LTD
Type
Standard
Approval Details
Approval Id
e1917a24715e3587
Product Name
PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH INFLAMMATION AND PAIN RELIEF ibuprofen sodium dihydrate 512 mg tablets blister pack
Artg Id
483928
Artg Name
PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH INFLAMMATION AND PAIN RELIEF ibuprofen sodium dihydrate 512 mg tablets blister pack
Sponsor
NOUMED PHARMACEUTICALS PTY LTD
Company Detail Path
/organization/noumed-pharmaceuticals-pty-ltd
Artg Date
2025-03-25
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
e1917a24715e3587
Type
Standard
Back to TGA Approvals