TGA Approval

APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack (217986)

ARTG ID

217986

ARTG Name

APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack

Sponsor

Arrotex Pharmaceuticals Pty Ltd

ARTG Date

February 20, 2014

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/4ab6ad030b2e7000112875cadc089056.pdf

https://medical-cdn.nocode.com/drug_tga/58a685cb40af9cd8c29c3d62ac771b78.pdf

Ingredient Name

duloxetine hydrochloride

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APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule blister pack (217986) - TGA 批准文号 | MedPath