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Veterinary Remove Veterinary filter
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Referral: Dexadreson
dexamethasone, Article 35
Status: European Commission final decision, opinion/position date: 18/07/2013, EC decision date: 18/10/2013, Last updated: 27/11/2013 -
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Referral: Micotil 300 Injectie
Tilmicosin, Article 34
Status: European Commission final decision, opinion/position date: 18/07/2013, EC decision date: 18/10/2013, Last updated: 20/11/2013 -
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Referral: Doramectin
doramectin, Article 35
Status: European Commission final decision, opinion/position date: 12/06/2013, EC decision date: 06/09/2013, Last updated: 18/10/2013 -
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Referral: Hipralona Enro-S
enrofloxacin, Article 35
Status: European Commission final decision, opinion/position date: 13/09/2012, EC decision date: 17/12/2012, Last updated: 04/02/2013 -
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Referral: Flukicides for which no maximum residue limit has been established in milk and which are intended for use in ruminants producing milk for human consumption
clorsulon, closantel, nitroxinil, rafoxanide, triclabendazole, Article 35
Status: European Commission final decision, opinion/position date: 14/06/2012, EC decision date: 19/11/2012, Last updated: 18/01/2013 -
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Referral: Baytril 10% oral solution
enrofloxacin, Article 34
Status: European Commission final decision, opinion/position date: 14/06/2012, EC decision date: 08/10/2012, Last updated: 20/11/2012 -
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Referral: Milaxyn Plus
praziquantel, pyrantel and febantel, associated names: Strantel Plus, Prazical Plus, Voxical Plus, Exitel Plus, Cazitel Plus and Prazitel Plus, Article 34
Status: European Commission final decision, opinion/position date: 07/03/2012, EC decision date: 18/06/2012, Last updated: 23/07/2012 -
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Referral: All pre-mixes for medicated feedingstuff containing 40 g, 100 g or 200 g tilmicosin per kg pre-mix and administered to rabbits
tilmicosin, associated names: See annex I, Article 35
Status: European Commission final decision, opinion/position date: 07/03/2012, EC decision date: 14/06/2012, Last updated: 19/07/2012 -
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Referral: Cephalosporins
ceftiofur and cefquinome, associated names: Cobactan, Cefenil, Ceftiocyl, Cevaxel, Eficur, Excenel, Readycef, Virbacef, Truleva, Ceftiomax, Ceftiosan, Actionis, Cemay, Article 35
Status: European Commission final decision, opinion/position date: 13/10/2011, EC decision date: 13/01/2012, Last updated: 01/02/2012 -
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Referral: Synulox Lactating Cow
amoxicillin trihydrate, potassium clavulanate, prednisolone, associated names: Avuloxil, Synulox LC, Synulox comp. vet, Synulox Endomammario, Article 34
Status: European Commission final decision, opinion/position date: 07/06/2011, EC decision date: 20/10/2011, Last updated: 17/11/2011 -
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Referral: Doxycycline 50% WSP
doxycycline hyclate, associated names: Doxymed 50, Vetadoxi 50, Doxylin Vet, Doxycycline Dophama, Article 34
Status: European Commission final decision, opinion/position date: 04/05/2011, EC decision date: 13/07/2011, Last updated: 24/08/2011 -
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Referral: Doxyfar 50%
doxycycline hyclate, associated names: Soludox 500 mg/g, Soludox Vet, Soludox 433 mg/g, Doxy Ort 50%, Article 34
Status: European Commission final decision, opinion/position date: 04/05/2011, EC decision date: 13/07/2011, Last updated: 24/08/2011 -
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Referral: Doxycycline hyclate
Doxycycline hyclate, Article 35
Status: European Commission final decision, opinion/position date: 11/02/2010, EC decision date: 14/06/2010, Last updated: 28/06/2011 -
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Referral: Tiamutin
Tiamulin hydrogen fumarate, Article 34
Status: European Commission final decision, opinion/position date: 10/03/2010, EC decision date: 27/07/2010, Last updated: 30/07/2010 -
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Referral: Quinolones
quinolones, Article 35
Status: European Commission final decision, opinion/position date: 09/03/2010, EC decision date: 01/07/2010, Last updated: 16/07/2010 -
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Referral: Colistin
Colistin sulfate, Article 35
Status: European Commission final decision, opinion/position date: 10/02/2010, EC decision date: 10/06/2010, Last updated: 24/06/2010 -
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Referral: Pulmotil AC
tilmicosin, Article 34
Status: European Commission final decision, opinion/position date: 16/07/2009, EC decision date: 15/10/2010, Last updated: 22/12/2009 -
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Referral: Pulmotil Premix
tilmicosin, Article 34
Status: European Commission final decision, opinion/position date: 16/07/2009, EC decision date: 15/10/2009, Last updated: 22/12/2009 -
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Referral: Ivermectin
Ivermectin, Article 35
Status: European Commission final decision, opinion/position date: 05/06/2009, EC decision date: 01/10/2009, Last updated: 26/10/2009 -
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Referral: Sodium Salicylate
Sodium salicylate, Article 35
Status: European Commission final decision, opinion/position date: 16/07/2008, EC decision date: 26/09/2008, Last updated: 19/11/2008 -
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Referral: Suramox 15 % LA and its associated name Stabox 15 % LA
Amoxicillin, associated names: Stabox 15% LA, Article 35
Status: European Commission final decision, opinion/position date: 18/06/2008, EC decision date: 05/09/2008, Last updated: 15/10/2008 -
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Referral: Methoxasol-T
trimethoprim and sulfamethoxazole, Article 34
Status: European Commission final decision, opinion/position date: 11/10/2007, EC decision date: 11/01/2008, Last updated: 09/10/2008 -
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Referral: Tribrissen
trimethoprim and sulfadiazine, Article 35
Status: European Commission final decision, opinion/position date: 12/12/2007, EC decision date: 11/03/2008, Last updated: 09/10/2008 -
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Referral: Toltrazuril
Toltrazuril, Article 35
Status: European Commission final decision, opinion/position date: 16/07/2008, EC decision date: 26/09/2008, Last updated: 26/07/2008 -
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Referral: Suramox
Amoxicillin, Article 35
Status: European Commission final decision, opinion/position date: 14/03/2007, EC decision date: 13/06/2007, Last updated: 25/07/2007