tulinovet
vmd n.v. - túlatrómýsín - antibacterials for systemic use, macrolides - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. tilvist sjúkdómsins í hjörðinni skal komið á áður en meðferð með bráðaofnæmi. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. tilvist sjúkdómsins í hjörðinni skal komið á áður en meðferð með bráðaofnæmi. the product should only be used if pigs are expected to develop the disease within 2–3 days. sauðfé: meðferð á fyrstu stigum smitandi beinbólgu (fótspyrnu) í tengslum við veirufræðilega dichelobacter nodosus sem krefst kerfisbundinnar meðferðar.
rexxolide
dechra regulatory b.v. - túlatrómýsín - sýklalyf til almennrar notkunar - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. tilvist sjúkdómsins í hjörðinni skal komið á áður en meðferð með bráðaofnæmi. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. tilvist sjúkdómsins í hjörðinni skal komið á áður en meðferð með bráðaofnæmi. the product should only be used if pigs are expected to develop the disease within 2–3 days. sauðfé: meðferð á fyrstu stigum smitandi beinbólgu (fótspyrnu) í tengslum við veirufræðilega dichelobacter nodosus sem krefst kerfisbundinnar meðferðar.
enteroporc coli ac
ceva santé animale - clostridium perfringens type c, beta1 toxoid / clostridium perfringens, type a, alpha toxoid / clostridium perfringens, type a, beta2 toxoid / escherichia coli, fimbrial adhesin f4ab / escherichia coli, fimbrial adhesin f4ac / escherichia coli, fimbrial adhesin f5 / escherichia coli, fimbrial adhesin f6 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - svín - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce:- clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6- clinical signs (diarrhoea during the first days of life) associated with clostridium perfringens type a expressing alpha and beta 2 toxins- clinical signs and mortality associated with haemorrhagic and necrotising enteritis caused by clostridium perfringens type c expressing beta1 toxin.
tramadol krka forðatafla 200 mg
krka, d.d., novo mesto - tramadolum hýdróklóríð - forðatafla - 200 mg
seroquel prolong forðatafla 50 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 50 mg
seroquel prolong forðatafla 300 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 300 mg
seroquel prolong forðatafla 200 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 200 mg
seroquel prolong forðatafla 150 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 150 mg
cernevit stungulyfsstofn, lausn
baxter medical ab* - vítamín a (palmítat); colecalciferolum inn; vítamín e (tocoferolum nfn); acidum ascorbicum inn; thiaminum cocarboxylase tetrahýdrat; riboflavinum natríumfosfat díhýdrat; pyridoxinum hýdróklóríð; cyanocobalaminum inn; acidum folicum inn; dexpanthenolum inn; biotinum inn; nicotinamidum inn - stungulyfsstofn, lausn
animed vet (anispray) húðúði, dreifa 2,45 % w/w
animedica gmbh* - chlortetracycline hydrochloride - húðúði, dreifa - 2,45 % w/w