0.5% Eprinomectin na-awụ na ngwọta
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Pharmacological omume
Eprinomectinbụ nke macrolide ụmụ ahụhụ, nke nwere mmetụta anthelmintic dị oke mma na nje ndị dị n'ime na mpụga, karịsịa nematodes na arthropods, site n'ịbawanye ntọhapụ nke γ-aminobutyric acid (γ-GABA), onye na-ebufe nje ahụ, yana imeghe glutamate. -Ọwa chloride a na-achịkwa, na-eme ka permeability nke akpụkpọ ahụ akwara na ion chloride iji gbochie nnyefe nke mgbaàmà akwara, n'ikpeazụ na-eduga na akwara ahụ mkpọnwụ nke nje na ọnwụ nke ikike nkwekọrịta nke mkpụrụ ndụ akwara na ọnwụ.
Pharmacological omume
Eprinomectinbụ soluble, na pharmacokinetics ya na-egosi njirimara ndị na-adịghị adị.Mgbe a wụsara 0.5 mg / kg · bw n'azụ anụ ehi mmiri ara ehi, ọnụ ọgụgụ kachasị elu (Cmax) bụ 18.64 ± 2.51 ng / ml, na oge ịkachasị elu (Tmax) bụ 3.63 ± 0.92 ụbọchị, pụtara oge obibi (MRT). ) 5.61 ± 0.45 ụbọchị, mpaghara n'okpuru usoro (AUC0-t) 113.90 ± 19.01 ng · ụbọchị ml, pụtara ìhè olu nkesa (Vd) 41 L, plasma mkpochapụ (CL) 4.5 L / ụbọchị, tumadi excreted na feces, na a obere ego a na-ewepụ na mmiri ara ehi na mmamịrị.
Ngosipụta
A na-eji Eprinomectin Pour on solution maka ọgwụgwọ ọrịa nje ndị dị ka nematodes na àjà in vitro na ehi mmiri ara ehi.
Usoro onunu ogwu na nchịkwa
A na-agbakọ ya dị ka Eprinomectin.Maka ojiji nke mpụga, jiri nwayọọ nwayọọ wụsa 0,5 mg ehi kwa 1 n'arọ nke ịdị arọ ahụ n'akụkụ azụ azụ nke ehi mmiri ara ehi site na ntu ruo n'isi ọdụ (ya bụ, 1 ml nke ngwaahịa a kwa kilogram 10 nke ịdị arọ ahụ).
Mkpachapụ anya
1. maka mpụga eji naanị anụ ụlọ.Akwụsịla ebe akpụkpọ ahụ nwere scabies, ọnya anụ ahụ, apịtị, na nsị.
2. Ọ bụrụ na ngwaahịa ahụ kpọnwụrụ akpọnwụ, ọ ga-agbaze kpamkpam ma maa jijiji nke ọma tupu ejiri ya.
3. Zere ikpughe ụmụaka na ọgwụ.
4. A ga-atụfu karama ọgwụ eji eme ihe na mmiri mmiri ọgwụ fọdụrụnụ (dịka olili ozu).
Mmeghachi omume ọjọọ
Mgbe ejiri ya na usoro a kapịrị ọnụ, ọ nweghị mmeghachi omume ọjọọ ahụghị.
Oge mwepụ
0 ụbọchị.
ngwugwu
200ml / karama, 1L / karama, 2L / karama, 5L / karama
Nchekwa
Chekwaa n'ọnọdụ mkpuchi n'okpuru 30 ℃, chebe ya pụọ na ìhè.
Hebei Veyong Pharmaceutical Co., Ltd, e guzobere na 2002, emi odude ke Shijiazhuang City, Hebei Province, China, na-esote Isi Obodo Beijing.Ọ bụ nnukwu ụlọ ọrụ ọgwụ anụmanụ enwetara ikike nke GMP, yana R&D, mmepụta na ire nke API ọgwụgwọ anụmanụ, nkwadebe, nri agbakwunyere na mgbakwunye nri.Dị ka Provincial Technical Center, Veyong eguzobela usoro R&D ọhụrụ maka ọgwụ anụmanụ ọhụrụ, ma bụrụ ụlọ ọrụ mmepụta ihe ọhụrụ na teknụzụ nke mba ama ama, enwere ndị ọkachamara teknụzụ 65.Veyong nwere abụọ mmepụta bases: Shijiazhuang na Ordos, nke Shijiazhuang isi na-ekpuchi ebe 78,706 m2, na 13 API ngwaahịa gụnyere Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, na 11 nkwadebe mmepụta akara gụnyere injection, oral ngwọta, ntụ ntụ ngwọta. , premix, bolus, pesticides na disinfectant, wdg.Veyong na-enye API, ihe karịrị 100 nkwado akara aha, yana ọrụ OEM & ODM.
Veyong na-etinye aka na njikwa nke sistemụ EHS (Environment, Health & Safety), ma nweta asambodo ISO14001 na OHSAS18001.Edepụtara Veyong n'ime ụlọ ọrụ mmepụta ihe na-emepụta atụmatụ dị na Hebei Province ma nwee ike hụ na ngwaahịa na-aga n'ihu.
Veyong guzobere usoro njikwa mma zuru oke, nweta asambodo ISO9001, asambodo China GMP, asambodo Australia APVMA GMP, asambodo Ethiopia GMP, asambodo Ivermectin CEP, wee gafere nyocha US FDA.Veyong nwere ọkachamara otu ndebanye aha, ahịa na ọrụ teknụzụ, ụlọ ọrụ anyị enwetala ntụkwasị obi na nkwado site n'aka ọtụtụ ndị ahịa site n'ịdị mma ngwaahịa dị mma, ọrụ tupu ire ere na mgbe ire ere, ọrụ siri ike na sayensị.Veyong emewo ogologo okwu imekọ ihe ọnụ na ọtụtụ mba ụwa maara na-emepụta ọgwụ ụlọ ọrụ na ngwaahịa exported na Europe, South America, Middle East, Africa, Asia, wdg karịa 60 mba na mpaghara.
