Pharmaceuticals - Community Register


Community register of veterinary medicinal products


Product information

Invented name: Recocam   
Auth. number : EU/2/11/133
Active substance : Meloxicam
ATC: Anatomical main group: QM - Musculo-skeletal system
Therapeutic subgroup: QM01 - Antiinflammatory and antirheumatic products
Pharmacological subgroup: QM01A - Antiinflammatory and antirheumatic products, non-steroids
Chemical subgroup: QM01AC - Oxicams
Chemical substance: QM01AC06 - meloxicam
(See WHO ATCvet Index)
Indication: Cattle
For use in acute respiratory infection with appropriate antibiotic therapy to reduce clinical signs in cattle.
For use in diarrhoea in combination with oral re-hydration therapy to reduce clinical signs in calves of over one week of age and young, non-lactating cattle.
For adjunctive therapy in the treatment of acute mastitis, in combination with antibiotic therapy.

For use in non-infectious locomotor disorders to reduce the symptoms of lameness and inflammation.
For adjunctive therapy in the treatment of puerperal septicaemia and toxaemia (mastitis-metritis-agalactia syndrome) with appropriate antibiotic therapy.

For use in the alleviation of inflammation and relief of pain in both acute and chronic musculo-skeletal disorders.
For the relief of pain associated with equine colic.
Marketing Authorisation Holder: Cross Vetpharm Group, Ltd
Broomhill Road, Tallaght Dublin 24, Ireland
EPAR and active package presentations

Package presentations

Information about presentations can be found in the website of the European Medicines Agency under the section "Product Information".
Likewise, presentations on which there has been a Commission decision are referred in the Summary of Product Characteristics (Annex I to the Commission Decision granting the marketing authorisation) which is available in the Community Register.

European Commission proceduresGoto top of the page

Close date procedure Procedure type EMEA number Decision summary publ decision docs annex
15/09/2011 Centralised - Authorisation EMEA/V/C/2247 (2011)6516 of 13/09/2011
12/02/2013 Centralised - Transfer Marketing Authorisation Holder EMEA/V/C/2247/T/1 (2013)798 of 08/02/2013
22/05/2013 Centralised - Variation EMEA/V/C/2247/IB/6
Updated with Decision(2014)3132 of 07/05/2014
29/05/2013 Centralised - Variation EMEA/V/C/2247/IB/2/G
Updated with Decision(2014)3132 of 07/05/2014
08/05/2014 Centralised - Yearly update (2014)3132 of 07/05/2014
11/08/2016 Centralised - Renewal EMEA/V/C/2247/R/8 (2016)5307 of 09/08/2016