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EMA Product

Pregabalin Zentiva

Product approved by European Medicines Agency (EU)

Basic Information

Pregabalin Zentiva

Regulatory Information

EMEA/H/C/003900

Authorised

July 17, 2015

May 21, 2015

18

October 17, 2024

Company Information

Czech Republic

U kabelovny 130 201 37 Prague 10

Zentiva, k.s.

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication **Neuropathic pain** - Pregabalin Zentiva is indicated for the treatment of peripheral and central neuropathic pain in adults. **Epilepsy** - Pregabalin Zentiva is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. **Generalised anxiety disorder** - Pregabalin Zentiva is indicated for the treatment of generalised anxiety disorder (GAD) in adults.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Pregabalin Zentiva. 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 Pregabalin Zentiva. For practical information about using Pregabalin Zentiva, patients should read the package leaflet or contact their doctor or pharmacist.

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