Zubrin

RSS
Withdrawn

This medicine's authorisation has been withdrawn

tepoxalin
MedicineVeterinaryWithdrawn
  • Application under evaluation
  • CVMP opinion
  • European Commission decision

Overview

The market authorisation for Zubrin has been withdrawn at the request of the marketing-authorisation holder.

Zubrin : EPAR - Summary for the public

English (EN) (510.23 KB - PDF)

First published: Last updated:
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español (ES) (511.13 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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čeština (CS) (595.78 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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dansk (DA) (510.17 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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Deutsch (DE) (513.33 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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eesti keel (ET) (510.33 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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ελληνικά (EL) (664.57 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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français (FR) (513.24 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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italiano (IT) (511.22 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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latviešu valoda (LV) (581.56 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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lietuvių kalba (LT) (536.1 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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magyar (HU) (589.67 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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Nederlands (NL) (510.07 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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polski (PL) (597.7 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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português (PT) (511.85 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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slovenčina (SK) (569.98 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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slovenščina (SL) (589.46 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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Suomi (FI) (510 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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svenska (SV) (509.65 KB - PDF)

First published: 23/05/2006 Last updated: 08/05/2012
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Product information

Zubrin : EPAR - Product Information

English (EN) (361.74 KB - PDF)

First published: Last updated:
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български (BG) (1.39 MB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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español (ES) (354.35 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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čeština (CS) (876.13 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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dansk (DA) (361.88 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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Deutsch (DE) (380.8 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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eesti keel (ET) (353.43 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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ελληνικά (EL) (1.1 MB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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français (FR) (363.75 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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íslenska (IS) (608.9 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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italiano (IT) (369.61 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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latviešu valoda (LV) (919.36 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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lietuvių kalba (LT) (1.36 MB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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magyar (HU) (1.04 MB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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Malti (MT) (898.07 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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Nederlands (NL) (369.61 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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norsk (NO) (663.7 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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polski (PL) (696.28 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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português (PT) (370.61 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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română (RO) (907.36 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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slovenčina (SK) (1.1 MB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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slovenščina (SL) (738.16 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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Suomi (FI) (347.73 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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svenska (SV) (339.08 KB - PDF)

First published: 14/02/2008 Last updated: 08/05/2012
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Latest procedure affecting product information:IB/0032
02/02/2012

Zubrin : EPAR - All Authorised presentations

English (EN) (243.39 KB - PDF)

First published: Last updated:
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español (ES) (243.72 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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čeština (CS) (768.39 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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dansk (DA) (243.34 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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Deutsch (DE) (460.26 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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eesti keel (ET) (15.67 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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ελληνικά (EL) (320.74 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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français (FR) (243.6 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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italiano (IT) (243.26 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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latviešu valoda (LV) (321.63 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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lietuvių kalba (LT) (304.46 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
View

magyar (HU) (308.89 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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Malti (MT) (322.75 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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Nederlands (NL) (243.75 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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polski (PL) (280.86 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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português (PT) (243.78 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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slovenčina (SK) (281.56 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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slovenščina (SL) (278.91 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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Suomi (FI) (240.48 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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svenska (SV) (244 KB - PDF)

First published: 27/03/2006 Last updated: 08/05/2012
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Product details

Name of medicine
Zubrin
Active substance
tepoxalin
International non-proprietary name (INN) or common name
tepoxalin
Species
Dogs
Anatomical therapeutic chemical veterinary (ATCvet) code
QM01AE92

Pharmacotherapeutic group

Musculo-skeletal system

Therapeutic indication

Reduction of inflammation and relief of pain caused by acute and chronic musculoskeletal disorders.

Authorisation details

EMA product number
EMEA/V/C/000057
Marketing authorisation holder
Intervet International BV

Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Marketing authorisation issued
13/03/2001
Revision
13

Assessment history

Zubrin : EPAR - Procedural steps taken and scientific information after authorisation

English (EN) (329.28 KB - PDF)

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Zubrin : EPAR - Scientific Discussion

English (EN) (444.01 KB - PDF)

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Zubrin : EPAR - Procedural steps taken before authorisation

English (EN) (235.23 KB - PDF)

First published: Last updated:
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