Approvals/TGA/PRILIGY dapoxetine 30 mg (as hydrochloride) film-coated tablet blister pack

Approved

STANDARD

PRILIGY dapoxetine 30 mg (as hydrochloride) film-coated tablet blister pack

A Menarini Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: ec312f5f080adc40
Product Name: PRILIGY dapoxetine 30 mg (as hydrochloride) film-coated tablet blister pack
Artg Id: 147946
Artg Name: PRILIGY dapoxetine 30 mg (as hydrochloride) film-coated tablet blister pack
Sponsor: A Menarini Australia Pty Ltd
Artg Date: 2010-09-02
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/0b6761279bce103fbdcf0c797411c9e7.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/b3104f7a5cb2e5660e9ff11365b5496b.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

ec312f5f080adc40

Type

Standard