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EMA Product

Levetiracetam Accord

Product approved by European Medicines Agency (EU)

Basic Information

Levetiracetam Accord

Regulatory Information

EMEA/H/C/002290

Authorised

October 3, 2011

July 21, 2011

19

April 30, 2025

Company Information

Spain

Edificio Este Planta 6a World Trade Center Moll De Barcelona S/n 08039 Barcelona

ACCORD HEALTHCARE SL

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Levetiracetam is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in patients from 16 years of age with newly diagnosed epilepsy. Levetiracetam is indicated as adjunctive therapy: - in the treatment of partial-onset seizures with or without secondary generalisation in adults, children and infants from one month of age with epilepsy; - in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy; - in the treatment of primary generalised tonic-clonic seizures in adults and adolescents from 12 years of age with idiopathic generalised epilepsy.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Levetiracetam Accord. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Levetiracetam Accord.

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