TGA Approval

DULOXETINE SANDOZ duloxetine (as hydrochloride) 30 mg enteric capsule blister pack (421536)

ARTG ID

421536

ARTG Name

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

Sponsor

Sandoz Pty Ltd

ARTG Date

August 13, 2024

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

Sandoz Pty Ltd.

https://medical-cdn.nocode.com/drug_tga/df5486719c3ebe735ad25a022b6806ad.pdf

https://medical-cdn.nocode.com/drug_tga/22992e3f94e58ea46d4608147643062d.pdf

Ingredient Name

duloxetine hydrochloride

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DULOXETINE SANDOZ duloxetine (as hydrochloride) 30 mg enteric capsule blister pack (421536) - TGA 批准文号 | MedPath