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Withdrawn application: Somnena
buprenorphine, date of withdrawal: 29/01/2016, Initial authorisation, Last updated: 14/09/2017 -
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Withdrawn application: Oxapex
date of withdrawal: 04/12/2014, Initial authorisation, Last updated: 29/07/2015 -
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Withdrawn application: Oncept Melanoma
date of withdrawal: 17/07/2014, Initial authorisation, Last updated: 24/02/2015 -
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Withdrawn application: Aivlosin
tylvalosin, date of withdrawal: 06/01/2014, Post-authorisation, Last updated: 21/07/2014 -
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Withdrawn application: Zolvix
monepantel, date of withdrawal: 19/10/2012, Post-authorisation, Last updated: 25/01/2013 -
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Withdrawn application: Draxxin
tulathromycin, date of withdrawal: 11/05/2012, Post-authorisation, Last updated: 04/07/2012 -
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Withdrawn application: Oxapex
date of withdrawal: 13/03/2012, Initial authorisation, Last updated: 25/06/2012 -
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Withdrawn application: Paccal Vet
paclitaxel, date of withdrawal: 02/03/2012, Initial authorisation, Last updated: 25/04/2012 -
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Withdrawn application: Zubrin
tepoxalin, date of withdrawal: 03/10/2008, Post-authorisation, Last updated: 24/02/2009 -
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Withdrawn application: Draxxin
tulathromycin, date of withdrawal: 17/01/2007, Post-authorisation, Last updated: 17/01/2007 -
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Withdrawn application: HopGuard Gold
date of withdrawal: 12/04/2018, Initial authorisation, Last updated: 26/11/2018 -
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Withdrawn application: Zydax
date of withdrawal: 03/12/2018, Initial authorisation, Last updated: 03/12/2018 -
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Withdrawn application: Coliprotec F4/F18
porcine post-weaning diarrhoea vaccine (live), date of withdrawal: 27/05/2019, Post-authorisation, Last updated: 18/09/2019 -
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Withdrawn application: Tulatrixx
tulathromycin, date of withdrawal: 01/04/2020, Initial authorisation, Last updated: 04/08/2020 -
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Withdrawn application: Equitend
date of withdrawal: 05/11/2018, Initial authorisation, Last updated: 01/04/2019 -
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Referral: Fortekor
benazepril hydrochloride, Article 34
Status: European Commission final decision, opinion/position date: 10/11/2011, EC decision date: 06/02/2012, Last updated: 11/03/2019 -
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Referral: Seresto and its associated name Foresto
imidacloprid and flumethrin, associated names: Foresto, Article 13
Status: European Commission final decision, opinion/position date: 15/02/2018, EC decision date: 25/05/2018, Last updated: 10/07/2018 -
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Referral: Girolan and its associated name Apralan
apramycin sulfate, associated names: Apralan, Article 34
Status: European Commission final decision, opinion/position date: 15/02/2018, EC decision date: 08/05/2018, Last updated: 15/06/2018 -
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Referral: Lincocin and its associated names
lincomycin, Article 34
Status: European Commission final decision, opinion/position date: 13/07/2017, EC decision date: 05/10/2017, Last updated: 14/11/2017 -
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Referral: Zanil and associated names, and generic products thereof
oxyclozanide, associated names: Zanil Suspension, Zanil Fluke Drench, Zanil Fluke Drench 34 mg/ml Oral Suspension, Article 35
Status: European Commission final decision, opinion/position date: 13/07/2017, EC decision date: 28/09/2017, Last updated: 25/10/2017 -
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Referral: Moxidectin-containing veterinary medicines used in cattle, sheep and horses
moxidectin, associated names: See annex I, Article 35
Status: European Commission final decision, opinion/position date: 11/05/2017, EC decision date: 26/09/2017, Last updated: 24/10/2017 -
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Referral: Zinc oxide
zinc oxide, Article 35
Status: European Commission final decision, opinion/position date: 16/03/2017, EC decision date: 26/06/2017, Last updated: 14/08/2017 -
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Referral: Denagard 45%
Tiamulin hydrogen fumarate, associated names: Tiamutin 45%, Denagard 450 mg/g, Denagard vet 450 mg/g, Article 34
Status: European Commission final decision, opinion/position date: 12/04/2017, EC decision date: 14/07/2017, Last updated: 11/08/2017 -
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Referral: Methylprednisolone injection for cattle
Methylprednisolone hydrogen succinate, Article 35
Status: European Commission final decision, opinion/position date: 16/03/2017, EC decision date: 20/06/2017, Last updated: 04/08/2017 -
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Referral: Tylosin injection for mastitis
tylosin, Article 35
Status: European Commission final decision, opinion/position date: 16/03/2017, EC decision date: 10/07/2017, Last updated: 31/07/2017