CircoMax Myco Uni Eropa - Islandia - EMA (European Medicines Agency)

circomax myco

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - Ónæmissjúkdómar fyrir suidae - svín (fyrir fitandi) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Suiseng Diff/A Uni Eropa - Islandia - EMA (European Medicines Agency)

suiseng diff/a

laboratorios hipra, s.a. - clostridioides difficile toxoid a, clostridioides difficile toxoid b, clostridium perfringens, type a, alpha toxoid - immunologicals for suidae, inactivated bacterial vaccines for pigs, clostridium - svín - for the passive immunisation of neonatal piglets by means of the active immunisation of breeding sows and gilts:- to prevent mortality and reduce clinical signs and macroscopic lesions caused by clostridioides difficile toxins a and b. - to reduce clinical signs and macroscopic lesions caused by clostridium perfringens type a, alpha toxin.

Vinorelbine Alvogen Mjúkt hylki 30 mg Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

vinorelbine alvogen mjúkt hylki 30 mg

alvogen pharma trading europe eood - vinorelbinum tvítartrat - mjúkt hylki - 30 mg

Eficur vet. Stungulyf, dreifa 50 mg/ml Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

eficur vet. stungulyf, dreifa 50 mg/ml

laboratorios hipra s.a.* - ceftiofurum hýdróklóríð - stungulyf, dreifa - 50 mg/ml

Prid delta Leggangainnlegg 1,55 g Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

prid delta leggangainnlegg 1,55 g

ceva santé animale* - progesteronum inn - leggangainnlegg - 1,55 g

Suiseng Vet Stungulyf, dreifa Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

suiseng vet stungulyf, dreifa

laboratorios hipra s.a.* - escherichia coli f4ab fimbrial adhesin; escherichia coli f4ac fimbrial adhesin; escherichia coli f5 fimbrial adhesin; escherichia coli f6 fimbrial adhesin; escherichia coli lt enterotoxoid; clostridium perfringens type-c beta toxoid; clostridium novyi toxoid - stungulyf, dreifa

Vetergesic vet. Stungulyf, lausn 300 míkróg/ml Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

vetergesic vet. stungulyf, lausn 300 míkróg/ml

ceva santé animale* - buprenorphinum hýdróklóríð - stungulyf, lausn - 300 míkróg/ml

Vetrimoxin L.A. Stungulyf, dreifa 150 mg/ml Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

vetrimoxin l.a. stungulyf, dreifa 150 mg/ml

ceva santé animale* - amoxicillinum tríhýdrat - stungulyf, dreifa - 150 mg/ml

Ferinject Stungulyf/innrennslislyf, ördreifa 50 mg/ml Islandia - Islandia - LYFJASTOFNUN (Icelandic Medicines Agency)

ferinject stungulyf/innrennslislyf, ördreifa 50 mg/ml

vifor france - ferricum carboxymaltosum inn - stungulyf/innrennslislyf, ördreifa - 50 mg/ml