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EMA Product

Pregabalin Sandoz

Product approved by European Medicines Agency (EU)

Basic Information

Pregabalin Sandoz

Regulatory Information

EMEA/H/C/004010

Authorised

June 19, 2015

April 23, 2015

21

November 22, 2024

Company Information

Austria

Biochemiestr. 10 6250 Kundl

Sandoz Gmbh

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication **Neuropathic pain** Pregabalin Sandoz is indicated for the treatment of peripheral and central neuropathic pain in adults. **Epilepsy** Pregabalin Sandoz is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. **Generalised Anxiety Disorder** Pregabalin Sandoz 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 Sandoz. 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 Sandoz. For practical information about using Pregabalin Sandoz, patients should read the package leaflet or contact their doctor or pharmacist.

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