Pregabalin

Pregabaline Zentiva 200 mg harde capsules

Capsule, hardNetherlandsAuthorisedAuthorised 17 Jul 2015

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In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

Pregabalin ZentivaEuropean UnionAuthorised

Documents

The official texts, at the regulator.

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

College ter Beoordeling van Geneesmiddelen

College ter Beoordeling van Geneesmiddelen, Geneesmiddeleninformatiebank metadata, source update 07-10-2026; downloaded 08-10-2026; factual adaptation.

Licence: Conditional noncreative administrative factual metadata; no dataset-wide CC0 claim · Added 8 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Pregabalin
Dosage form: Capsule, hard
Route: Oraal gebruik
Register: Netherlands (CBG-MEB)
Status: Authorised
Status in the register: Ingeschreven
Authorised: 17 Jul 2015
Registration: EU/1/15/1021
Marketing authorisation holder: Zentiva k.s.
ATC code: N02BF02
Group: Nervous system
Procedure: EU centralised
Supply: Uitsluitend recept
EMA product number: EMEA/H/C/003900
EU number: EU/1/15/1021

Pregabaline Zentiva 200 mg harde capsules

In other countries

Authorised centrally in the EU

Documents

Sources and licences

At a glance

Two medicines in one question?

Pregabaline Zentiva 200 mg harde capsules

In other countries

Authorised centrally in the EU

Documents

Sources and licences

At a glance

Two medicines in one question?