Ireland - English - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - cefuroxime sodium - pdr for soln for injection - 250 base milligrams - second-generation cephalosporins

Ireland - English - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - cefuroxime sodium - pdr for soln for injection - 750 base milligrams - second-generation cephalosporins

Ireland - English - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - cefuroxime sodium (sterile) - pdr for soln inj/inf - 1.5 grams - second-generation cephalosporins

Austria - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

Greece - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

Spain - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

France - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

Hungary - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

Portugal - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin

United Kingdom - English - HMA (Heads of Medicines Agencies)

virbac s.a. - ceftiofur 1000 mg, ceftiofur 4000 mg - powder for solution for injection - cattle, horses, pigs - cefalexin