Product details

Commercial name Actionis 50 mg/ml
Authorization number 190322
Authorization status Valida
Authorization date 16-12-2019
Authorization valid date 16-12-2024
Active substance ceftiofur clorhidrat
Target species bovine, porcine
Therapeutical action Bovine şi porcine Tratamentul infecţiilor produse de microorganisme sensibile la ceftiofur.
Therapeutic group Antibiotice
Pharmaceutical form suspensie injectabilă
Packaging flacon x 100 ml, 250 ml
Withdrawal period Carne şi organe: bovine - 6 zile, porcine - 6 zile. Lapte: 0 ore.
Manufacturer LABORATORIOS SYVA S.A.U., Spania
Licence owner DEAVET SRL, România
Romanian responsible company DEAVET SRL
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Link to authorization
Notes Autorizaţie de import paralel (produsul din ţara de origine: ACTIONIS 50 mg/ml al firmei LABORATORIOS SYVA - Spania; produsul de referinţă din România: CEVAXEL RTU mg/ml al firmei CEVA SANTE ANIMALE - Franţa).
Release Mode Cu prescripţie
Authorizations history
Commercial name Authorization number Authorization date Authorization valid date Authorization status
Actionis 50 mg/ml 140192 09-09-2014 09-09-2019 Expirata