Approvals/TGA/DULOXETINE SANDOZ duloxetine (as hydrochloride) 60 mg enteric capsule blister pack

Approved

STANDARD

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

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f7636292f8faea77
Product Name: DULOXETINE SANDOZ duloxetine (as hydrochloride) 60 mg enteric capsule blister pack
Artg Id: 421530
Artg Name: DULOXETINE SANDOZ duloxetine (as hydrochloride) 60 mg enteric capsule blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2024-08-13
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/df5486719c3ebe735ad25a022b6806ad.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/22992e3f94e58ea46d4608147643062d.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

f7636292f8faea77

Type

Standard