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NOUMED TERBINAFINE 250 terbinafine (as hydrochloride) 250 mg tablet blister pack - TGA Drug Approval Details
Approvals
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TGA
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NOUMED TERBINAFINE 250 terbinafine (as hydrochloride) 250 mg tablet blister pack
Approved
STANDARD
NOUMED TERBINAFINE 250 terbinafine (as hydrochloride) 250 mg tablet blister pack
Avallon Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
c069f7aafb58785a
Company
Avallon Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
c069f7aafb58785a
Product Name
NOUMED TERBINAFINE 250 terbinafine (as hydrochloride) 250 mg tablet blister pack
Artg Id
324497
Artg Name
NOUMED TERBINAFINE terbinafine (as hydrochloride) 250 mg tablet blister pack
Sponsor
Avallon Pharmaceuticals Pty Ltd
Company Detail Path
/organization/avallon-pharmaceuticals-pty-limited
Artg Date
2019-12-13
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/7c04d228ab78e258c559c2a110c4c1a7.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/f421540ac41af3353d3e06cbf27c2b45.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
c069f7aafb58785a
Type
Standard
Back to TGA Approvals