TGA Approval

NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 10 mg immediate release tablet blister pack (311725)

ARTG ID

311725

ARTG Name

NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 10 mg immediate release tablet blister pack

Sponsor

Southern Cross Pharma Pty Ltd

ARTG Date

April 3, 2020

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

SOUTHERN CROSS PHARMA PTY LTD

https://medical-cdn.nocode.com/drug_tga/26a6306c864737b9c8545810934012a0.pdf

https://medical-cdn.nocode.com/drug_tga/d15bb4167d7715c9e1e266848e77d8d3.pdf

Ingredient Name

nebivolol hydrochloride

Empowering clinical research with data-driven insights and AI-powered tools.

NEBIVOLOL SANDOZ nebivolol (as hydrochloride) 10 mg immediate release tablet blister pack (311725) - TGA 批准文号 | MedPath