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LOBIVON nebivolol (as hydrochloride) 1.25mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
LOBIVON nebivolol (as hydrochloride) 1.25mg tablet blister pack
Approved
STANDARD
LOBIVON nebivolol (as hydrochloride) 1.25mg tablet blister pack
A Menarini Australia Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
108cb442f0ba389f
Company
A Menarini Australia Pty Ltd
Type
Standard
Approval Details
Approval Id
108cb442f0ba389f
Product Name
LOBIVON nebivolol (as hydrochloride) 1.25mg tablet blister pack
Artg Id
148877
Artg Name
LOBIVON nebivolol (as hydrochloride) 1.25mg 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
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
108cb442f0ba389f
Type
Standard
Back to TGA Approvals
