20% tylosin tarrate jekiseni
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Kuumbwa
Imwe neimwe 1ML ine: tylosin (se tarrate) 200mg
Chiratidzo
20% tylosin tarrate jekiseniaigona kurapa hutachiona hwakakonzerwa nemakiromita anokonzerwa ne tylosin, sengefomu ekufema turakiti, mapopoma uye dysentery uye arthritis yakakonzerwa neyemycoplasmas, mastitis uye endometriti.
Contincu-inoratidza hypersensitivity kune tylosin, kuyambuka-hyperssions-tivity to macrodides.
Dosage uye Administration
Yemitambo intraustar kana subcutaneous.
Mombe: 0.5-1 ML pa 10 KG muviri muviri zuva nezuva, mukati memazuva 3-5.
Mhuru, makwai, mbudzi: 1.5-2 ML paChirimba makumi mashanu nemashanu, mukati memazuva 3-5.
Nguruve: 0.5-0.75 ml pagumi kg muviri wese gumi nemaviri, mukati memazuva matatu.
Imbwa, katsi: 0.5-2 ml pagumi kg bodyweight zuva nezuva, mukati memazuva 3-5.
Mhedzisiro
Zvakanyanya kujairika ndeyekuita kwenzvimbo panzvimbo ye jekiseni.
Kubviswa nguva
Nyama Yekushandisa Kwevanhu: Mazuva masere
Mukaka wekushandisa kwevanhu: Mazuva mana.
Chitarisiko
Isina ruvara kana zvishoma yero yakajeka mvura.
Chengetedza
Chengetedza munzvimbo inotonhorera, yakaoma.
HEBEI VEYONG PHEMACALUTICAL CO, LTD, yakagadzwa muna 2002, iri muShijizhuang Guta, HEBEI Province, China, padivi peguta guru beijing. Iye iguru rakakura Sezvo provencial technical centre, veyong yakaisa iyo yeRidheni yeR & D yechiitiko chevateridzi, uye ndiyo inozivikanwa yerudzi runyorwa rwehunyanzvi hwenostical Veyong ine zvigadziko zviviri zvekugadzira: Shijizhuang uye yeiyo iyo Shijizhuang base inovhara maHydrochlar, Bolus, mishonga yechipfuva uye disinfectant, ects. Veyong inopa apis, inodarika 100 yekugadzirira, uye OEM & ODM Service.
Veyong anotsvaga kukosha kukuru kune manejimendi eEHS (nharaunda, hutano & kuchengetedza) system, uye yakawana iyo iso1001 uye OHSAS18001 zvitupa. Veyong yakanyorwa mumarongero emunguva inobuda mumabhizimusi muHebeid muBedi Province uye anogona kuve nechokwadi chekuisa kugovera kwezvigadzirwa.
Veyong vakatanga iyo yakazara mhando yemhando system, yakawana iyo SOO9001 Setifiketi, China GRMS Setifiketi, Australia Apm Setififiketi, Ivermectin Cepictate, uye yadarika US FDA kuongorora. Veyong vane nyanzvi yekudzikama, kutengesa uye technical service, yedu tsigiro kubva kune vatengi vakawanda neiyo yechigadzirwa chechigadzirwa, yakakwirira-nzira yekutengesa uye mushure mekutengesa-mutengesi, manejimendi uye akakosha uye ane ruzivo uye manejimendi. Veyong vakawana nguva refu kushandira pamwe nevazhinji vanozivikanwa emaperembudzi ezvivakwa nezvigadzirwa zvinotumirwa kuEurope, South America, Middle East, Africa, etc., etc. dzinopfuura nyika makumi matanhatu nematunhu.
