MedPath
EMA Product

Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen)

Product approved by European Medicines Agency (EU)

Basic Information

Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen)

Regulatory Information

EMEA/H/C/003803

Authorised

June 30, 2015

April 23, 2015

18

May 22, 2024

Company Information

Ireland

Damastown Industrial Park Mulhuddart Dublin 15

MYLAN PHARMACEUTICALS PRIVATE LIMITED

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Aripiprazole Mylan Pharma is indicated for the treatment of schizophrenia in adults and in adolescents aged 15 years and older. Aripiprazole Mylan Pharma is indicated for the treatment of moderate to severe manic episodes in Bipolar I Disorder and for the prevention of a new manic episode in adults who experienced predominantly manic episodes and whose manic episodes responded to aripiprazole treatment. Aripiprazole Mylan Pharma is indicated for the treatment up to 12 weeks of moderate to severe manic episodes in Bipolar I Disorder in adolescents aged 13 years and older.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Aripiprazole Mylan Pharma. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Aripiprazole Mylan Pharma. For practical information about using Aripiprazole Mylan Pharma, patients should read the package leaflet or contact their doctor or pharmacist.

© Copyright 2025. All Rights Reserved by MedPath