12.5% Amitraz Solution
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Tulaga
O ml taʻitasi e aofia ai Amitraz 125 mg
Fa'ailoga
12.5% fofo Amitraze mo le puipuia ma le fa'atonutonuina o fa'ama'i pipisi ectoparasitic e pei o Ticks, Mange mites, utu fa'apea ma povi, Kamela, Mamoe, 'oti ma Pua.Ole vaifofo a Amitraz e mafai ona fa'amateina fa'ama'i, manu iti ma utu e aofia ai ma'i e tete'e ile organochlorines, organophosphates ma pyrethroids synthetic.
Contraindications
E le fautuaina lenei oloa mo le fa'aoga i ituaiga o maile, Pusi & Chihuahua.
Fuafuaga ma le Pulega
12.5% Amitraz solution e mafai ona faʻaaogaina e pei o le faʻafefe poʻo le togi
amitraz 12.5% vaifofo o vai mo siaki, mites (mange), utu ma keds
povi/kamela: 2.0 ml
Mamoe/'oti: 4.0 ml
puaa: 4.0 ml
Sauni le faʻafefe i le aso o togafitiga e faʻaaoga ai vai mama.Fai i se vaega i le taimi e tasi ia togafiti uma ma manu e le afaina.
Fa'amatalaga
I tulaga ogaoga o le manumanu poʻo le utu, e fautuaina le togafitiga lona lua i le 7-10 aso talu ona maeʻa togafitiga muamua
Taimi Aveesea
Aano o manufasi- 1 aso mo povi ma 'oti ma 7 aso mo puaa ma susu susu- 4 susu / 2 aso
Teuina
Teu i totonu o le koneteina muamua e tapunia lelei i se nofoaga saogalemu e mamao ese mai meaʻai.Teu malu puipuia mai le malamalama
Hebei Veyong pharmaceutical Co., Ltd, na faavaeina i le 2002, o loʻo i Shijiazhuang City, Hebei Province, Saina, i tafatafa o le Laumua Beijing.O ia o se GMP-certified veterinary drug enterprise, faʻatasi ai ma le R&D, gaosiga ma le faʻatau atu o veterinary APIs, sauniuniga, meaʻai muamua ma meaʻai faaopoopo.I le avea ai o le Nofoaga Tutotonu Faʻatekonolosi Faʻatekonolosi, ua faʻatūina e Veyong se faiga fou R & D mo vailaʻau faʻasoifua fou, ma o le atunuʻu lauiloa faʻatekonolosi faʻavae atinaʻe vailaʻau, e 65 tagata tomai faʻapitoa.Veyong e lua faavae gaosiga: Shijiazhuang ma Ordos, lea o le Shijiazhuang faavae e aofia ai se vaega o le 78,706 m2, ma 13 oloa API e aofia ai Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, ma 11 saunia laina gaosiga e aofia ai tui, fofo tautala, paʻu. , premix, bolus, vailaau e tineia ai manu faalafua ma vailaau fa'ama'i, ma isi.Veyong e tu'uina atu API, sili atu i le 100 lava-igoa sauniuniga, ma OEM & ODM auaunaga.
Veyong faʻapipiʻi taua tele i le pulega o le EHS (Siosiomaga, Soifua Maloloina & Saogalemu), ma maua le ISO14001 ma OHSAS18001 tusi pasi.Veyong ua lisiina i totonu o atinaʻe faʻapisinisi faʻapitoa faʻapitoa i le Itumalo o Hebei ma e mafai ona faʻamautinoa le faʻaauau pea o oloa.
Veyong faʻatūina le faʻatonuga lelei atoatoa, maua le ISO9001 tusi pasi, Saina GMP tusi faamaonia, Ausetalia APVMA GMP tusi faamaonia, Etiopia GMP tusi faamaonia, Ivermectin CEP tusi faamaonia, ma pasia US FDA asiasiga.Veyong ei ai le 'au faʻapolofesa o le resitalaina, faʻatau ma auaunaga faʻapitoa, ua maua e le matou kamupani le faʻalagolago ma le lagolago mai le tele o tagata faʻatau e ala i le tulaga lelei o oloa, maualuga le faʻatau atu ma le maeʻa o le faʻatau atu, pulega ogaoga ma faasaienisi.Veyong ua faia le galulue faatasi mo se taimi umi ma le tele o pisinisi faava o malo pharmaceutical manu ma oloa auina atu i fafo i Europa, Amerika i Saute, Sasaʻe Tutotonu, Aferika, Asia, ma isi e sili atu i le 60 atunuu ma itulagi.
