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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

Arrotex Pharmaceuticals Pty Ltd

Sponsor Item Name

Arrotex Pharmaceuticals Pty Ltd.

Product Information

Consumer Medicine Information

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

Product Information

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

Active Ingredients

Ingredient Name

duloxetine hydrochloride

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