TGA Approval

APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack (427036)

ARTG ID

427036

ARTG Name

APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

Sponsor

Arrotex Pharmaceuticals Pty Ltd

ARTG Date

September 20, 2024

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

Arrotex Pharmaceuticals Pty Ltd.

https://medical-cdn.nocode.com/drug_tga/fb762eb24cc9af8eee316bda31446a69.pdf

https://medical-cdn.nocode.com/drug_tga/e83fd6748c3770f71e1f2d1197eef865.pdf

Ingredient Name

duloxetine hydrochloride

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

APO-DULOXETINE duloxetine (as hydrochloride) 30 mg enteric capsule blister pack (427036) - TGA 批准文号 | MedPath