Írsko - angličtina - HPRA (Health Products Regulatory Authority)

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

Írsko - angličtina - HPRA (Health Products Regulatory Authority)

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

Írsko - angličtina - HPRA (Health Products Regulatory Authority)

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

Rakúsko - angličtina - HMA (Heads of Medicines Agencies)

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

Grécko - angličtina - HMA (Heads of Medicines Agencies)

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

Španielsko - angličtina - HMA (Heads of Medicines Agencies)

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

Francúzsko - angličtina - HMA (Heads of Medicines Agencies)

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

Maďarsko - angličtina - HMA (Heads of Medicines Agencies)

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

Portugalsko - angličtina - HMA (Heads of Medicines Agencies)

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

Spojené kráľovstvo - angličtina - HMA (Heads of Medicines Agencies)

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