0.5% Eprinomectin Zuba Magani

Takaitaccen Bayani:

Manyan abubuwa:

Kowane 100ml ya ƙunshi 0.5gEprinomectin.

Lokacin janyewa: kwanaki 0.

Marka: VEYONG,

Sabis: OEM & ODM

Amfani: Don amfanin waje

Kunshin: 200ml / kwalban, 1L / kwalban, 2L / kwalban, 5L / kwalban


Farashin FOB US $0.5 - 9,999 / yanki
Min. Yawan oda 1 Yanki/Kashi
Ƙarfin Ƙarfafawa 10000 Pieces/Perces per month
Lokacin biyan kuɗi T/T, D/P, D/A, L/C
rakumai shanu awaki tumaki aladu

Cikakken Bayani

Bayanin Kamfanin

Tags samfurin

Pharmacological mataki

Eprinomectinyana cikin magungunan kwari na macrolide, waɗanda ke da tasirin anthelmintic sosai a kan ƙwayoyin cuta na ciki da na waje, musamman nematodes da arthropods, ta hanyar haɓaka sakin γ-aminobutyric acid (γ-GABA), mai watsawa mai hana ƙwayoyin cuta, da buɗe glutamate. -tashoshin chloride mai sarrafa, yana haɓaka haɓakar membrane na jijiyar zuwa ions chloride don toshe watsa siginar jijiya, wanda hakan ke haifar da gurɓataccen jijiya na ƙwayar cuta da asarar ƙarfin kwangilar ƙwayoyin tsoka da mutuwa.

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Pharmacological mataki

Eprinomectinyana narkewa, kuma magungunan sa na pharmacokinetic yana nuna halaye marasa daidaituwa.Lokacin da aka zubar da 0.5 mg / kg · bw a baya na shanun kiwo, mafi girman maida hankali (Cmax) shine 18.64 ± 2.51 ng / ml, kuma lokacin da za a yi girma (Tmax) shine 3.63 ± 0.92 kwanaki, yana nufin lokacin zama (MRT). ) 5.61 ± 0.45 kwanaki, yanki a karkashin lankwasa (AUC0-t) 113.90 ± 19.01 ng · day ml, bayyanannun girma na rarraba (Vd) 41 L, plasma yarda (CL) 4.5 L / rana, yafi excreted a cikin feces, da kuma karamin adadin da ake fitarwa a cikin madara da fitsari. 

Nuni

Ana amfani da Eprinomectin Pour akan bayani don maganin cututtukan cututtuka irin su nematodes da mites in vitro a cikin shanun kiwo.

Sashi da Gudanarwa

An ƙididdige shi azaman Eprinomectin.Don amfani da waje, a hankali zuba 0.5 MG na shanu a kowace kilogiram 1 na nauyin jiki tare da dorsal ridge na shanun kiwo daga ƙusa zuwa tushe na wutsiya (watau 1 ml na wannan samfurin a kowace kilogiram 10 na nauyin jiki).

zuba a kan bayani

Matakan kariya

1. don amfanin waje a cikin dabbobi kawai.Kada a shafa a wuraren fata masu ƙumburi, raunin fata, laka, da najasa.
2. Idan samfurin ya daskare, ya kamata a narke gaba ɗaya kuma a girgiza sosai kafin amfani.
3. A guji shan miyagun kwayoyi ga yara.
4. kwalaben magani da aka yi amfani da su da sauran ruwan magani za a zubar da su lafiya (kamar binnewa).

Mummunan halayen

Lokacin da aka yi amfani da shi a ƙayyadaddun kashi, ba a ga wani mummunan halayen ba.

Lokacin janyewa

kwanaki 0.

Kunshin

200ml / kwalban, 1L / kwalban, 2L / kwalban, 5L / kwalban

Adana

Ajiye a cikin yanayin rufe ƙasa ƙasa da 30 ℃, an kiyaye shi daga haske.


  • Na baya:
  • Na gaba:

  • https://www.veyongpharma.com/about-us/

    Hebei Veyong Pharmaceutical Co., Ltd, an kafa shi a shekara ta 2002, wanda yake a birnin Shijiazhuang na lardin Hebei na kasar Sin, kusa da babban birnin Beijing.Ita babbar sana'ar sayar da magungunan dabbobi ce ta GMP, tare da R&D, samarwa da tallace-tallace na APIs na dabbobi, shirye-shirye, ciyarwar da aka riga aka haɗa da ƙari.A matsayin Cibiyar Fasaha ta Lardi, Veyong ya kafa sabon tsarin R&D don sabbin magungunan dabbobi, kuma shine sanannen masana'antar fasahar kere kere ta ƙasa, akwai kwararrun fasaha 65.Veyong yana da biyu samar sansanonin: Shijiazhuang da Ordos, wanda Shijiazhuang tushe maida hankali ne akan wani yanki na 78,706 m2, tare da 13 API kayayyakin ciki har da Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, da kuma 11 shiri samar Lines ciki har da allura, ko foda bayani. , premix, bolus, magungunan kashe qwari da magungunan kashe qwari, da sauransu.Veyong yana ba da APIs, fiye da shirye-shiryen alamar mallaka 100, da sabis na OEM & ODM.

    Veyong (2)

    Veyong yana ba da mahimmanci ga gudanar da tsarin EHS (Muhalli, Lafiya & Tsaro), kuma ya sami takaddun shaida na ISO14001 da OHSAS18001.An jera Veyong a cikin dabarun masana'antu masu tasowa a lardin Hebei kuma yana iya tabbatar da ci gaba da samar da kayayyaki.

    HEBEI VEYONG
    Veyong ya kafa cikakken tsarin gudanarwa mai inganci, ya sami takardar shedar ISO9001, takardar shaidar GMP ta kasar Sin, takardar shedar APVMA GMP ta Australia, takardar shaidar GMP ta Habasha, takardar shaidar Ivermectin CEP, kuma ta wuce binciken FDA na Amurka.Veyong yana da ƙwararrun ƙungiyar rajista, tallace-tallace da sabis na fasaha, kamfaninmu ya sami dogaro da goyan baya daga abokan ciniki da yawa ta kyakkyawan ingancin samfur, ingantaccen pre-tallace-tallace da sabis na tallace-tallace, mai tsanani da sarrafa kimiyya.Veyong ya yi dogon lokaci hadin gwiwa tare da da yawa duniya sanannun dabbobi Pharmaceutical Enterprises tare da kayayyakin da ake fitarwa zuwa Turai, Kudancin Amirka, Gabas ta Tsakiya, Afirka, Asiya, da dai sauransu fiye da 60 kasashe da yankuna.

    Farashin VEYONG PHARMA

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