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TGA
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NEBILET nebivolol (as hydrochloride) 5mg tablet blister pack
Approved
STANDARD
NEBILET nebivolol (as hydrochloride) 5mg tablet blister pack
A Menarini Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
b2a437b16fe508d4
Company
A Menarini Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
b2a437b16fe508d4
Product Name
NEBILET nebivolol (as hydrochloride) 5mg tablet blister pack
Artg Id
148874
Artg Name
NEBILET nebivolol (as hydrochloride) 5mg tablet blister pack
Sponsor
A Menarini Australia Pty Ltd
Artg Date
2009-06-26
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/c6e2652c7c0d71873ca226747f667006.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/7b366c3a6853352b671757af16d195e9.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
b2a437b16fe508d4
Type
Standard
Back to TGA Approvals
NEBILET nebivolol (as hydrochloride) 5mg tablet blister pack - TGA Drug Approval Details
