26 October 2017 EMA/722496/2017 Human Medicines Evaluation Division

List of nationally authorised medicinal products

Active substance: hydroquinidine

Procedure no.: PSUSA/00001688/201703

30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5525 Send a question via our website www.ema.europa.eu/contact

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© European Medicines Agency, 2017. Reproduction is authorised provided the source is acknowledged.

Product Name (in authorisation

MRP/DCP

National Authorisation

MAH of product in

Member State where

country)

Authorisation number

Number

the member state

product is authorised

Hidroquinidina Serecor 300 mg cápsulas

FR/H/0585/001

79946

SANOFI-AVENTIS, S.A.

ES

FR/H/0585/001

79946

SANOFI-AVENTIS, S.A.

ES

FR/H/0585/001

324 007-0

SANOFI-AVENTIS

FR

duras de liberación polongada Hidroquinidina Serecor 300 mg cápsulas duras de liberación polongada SERECOR 300 mg, gélule à libération prolongée SERECOR 300 mg, gélule à libération

FRANCE FR/H/0585/001

324 008-7

prolongée IDROCHINIDINA LIRCA 150 mg

SANOFI-AVENTIS

FR

FRANCE not available

005494024

TEOFARMA S.R.L.

IT

not available

023165018

TEOFARMA S.R.L.

IT

compresse IDROCHINIDINA RITARDO LIRCAPS 250 mg capsule rigide a rilascio prolungato

List of nationally authorised medicinal products EMA/604559/2017

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hydroquinidine PSUSA 00001688 201703 - European Medicines ...

Oct 26, 2017 - Human Medicines Evaluation Division. List of nationally authorised medicinal products. Active substance: hydroquinidine. Procedure no.
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