Approvals/TGA/FYCOMPA perampanel (as hemisesquihydrate) 8 mg film coated tablet blister

Approved

STANDARD

FYCOMPA perampanel (as hemisesquihydrate) 8 mg film coated tablet blister

Eisai Australia Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 9fe5bd637ae9d1fb
Product Name: FYCOMPA perampanel (as hemisesquihydrate) 8 mg film coated tablet blister
Artg Id: 207687
Artg Name: FYCOMPA perampanel (as hemisesquihydrate) 8 mg film coated tablet blister
Sponsor: Eisai Australia Pty Ltd
Company Detail Path: /organization/eisai-australia-pty-ltd
Artg Date: 2014-05-23
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/b220651ea908dcc04416cb2f97176b2b.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/3829f909b7e089dc55600162e3cc3b8b.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

9fe5bd637ae9d1fb

Type

Standard