5% Diclofenac Sodium jakisoni wogwiritsa ntchito nyama

Kufotokozera Kwachidule:

Zolemba:

ml iliyonse imakhala ndi Diclofenac Sodium 50mg

Phukusi:

10ml / vial, 20ml / vial, 50ml / botolo,

100ml / botolo, 250ml / botolo, 500ml / botolo

Service:OEM & ODM

Chitsanzo:Zopezeka


Mtengo wapatali wa magawo FOB US $ 0.5 - 9,999 / Chigawo
Min.Order Kuchuluka 1 Chidutswa / Zidutswa
Kupereka Mphamvu 10000 Chidutswa/Zidutswa pamwezi
Nthawi yolipira T/T, D/P, D/A, L/C
ngamila ng'ombe nkhumba mbuzi nkhosa

Tsatanetsatane wa Zamalonda

Mbiri Yakampani

Zogulitsa Tags

Kupanga

ml iliyonse imakhala ndi Diclofenac Sodium 50mg

Katundu:

Diclofenac sodium, sodium 2- [(2,6-dichlorophenyl) amino] phenylacetate ndi imodzi mwa mankhwala osagwiritsidwa ntchito poletsa kutupa (NSAIDs), ndi ya phenyl acetic acid derivatives.Diclofenac sodium monga odana ndi kutupa, analgesic ndi antipyretic zotsatira ndi chifukwa cha kuchepa kwa kaphatikizidwe prostaglandin kuchokera arachidonic acid ndi chopinga wa cyclo-oxygenase.Zotsatira zake ndi 2 ~ 2.5 nthawi zamphamvu kuposa indomethacin ndi 26 ~ 50 nthawi zamphamvu kuposa acetylsalicylic acid.Amadziwika ndi mphamvu yamankhwala yamphamvu, kusagwirizana kwapang'onopang'ono, mlingo waung'ono, ndi zosiyana zazing'ono.

Kumangirira kwa mankhwalawa ku mapuloteni a plasma ndi 99.7%.Hafu ya moyo ndi 1 mpaka 2 hours.Malinga ndi mlingo woyenera ndi nthawi, palibe kudzikundikira.Mankhwala zimapukusidwa ndi chiwindi, ndipo pafupifupi 60% ya achire kuchuluka kwa metabolites excreted ku impso, ndi excretion wa mankhwala oyambirira ndi zosakwana 1%.Mlingo wotsalawo uli mu mawonekedwe a metabolites, omwe amatulutsidwa m'matumbo kudzera mu ndulu, ndikuchotsedwa mu ndowe.jekeseni wa sodium diclofenac

Zizindikiro

Antipyretic analgesics.Diclofenac sodium jekeseni monga odana ndi yotupa ndi analgesic, akusonyeza kulamulira ululu ndi kutupa kugwirizana ndi matenda a minofu ndi mafupa monga;nyamakazi, nyamakazi, osteochondritis, bursitis, tendenitis ndi myositis, chibayo pachimake, pachimake mastitis ndi enteritis.

Amagwiritsidwanso ntchito powongolera kutentha thupi komwe kumakhudzana ndi matenda kapena kuwonongeka kwa minofu mumitundu yosiyanasiyana ya nyama.

Mlingo ndi Kuwongolera

Jekeseni mu mnofu:

mlingo umodzi, 1.25mg pa 1kg kulemera kwa thupi;

nyama mosalekeza ntchito 1-3 masiku.

Kusamalitsa:Iyenera kubayidwa pang'onopang'ono.

Kusungirako: Sungani pamalo ozizira, owuma ndi amdima.Khalani kutali ndi ana.


  • Zam'mbuyo:
  • Ena:

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

    Hebei Veyong pharmaceutical Co., Ltd, unakhazikitsidwa mu 2002, ili mu Shijiazhuang City, Hebei Province, China, pafupi ndi Capital Beijing.Ndi kampani yayikulu yovomerezeka ya GMP yotsimikizira za Chowona Zanyama, yokhala ndi R&D, kupanga ndi kugulitsa ma API a Chowona Zanyama, kukonzekera, zakudya zosakaniza ndi zowonjezera zowonjezera.Monga Provincial Technical Center, Veyong yakhazikitsa njira yatsopano ya R&D yamankhwala atsopano azowona zanyama, ndipo ndi kampani yodziwika bwino yaukadaulo yozikidwa pazanyama, pali akatswiri 65 aukadaulo.Veyong ili ndi zoyambira ziwiri zopangira: Shijiazhuang ndi Ordos, pomwe maziko a Shijiazhuang amatenga malo a 78,706 m2, okhala ndi zinthu 13 za API kuphatikiza Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, ndi 11, mizere yopangira jekeseni, njira yopangira jekeseni. , premix, bolus, mankhwala ndi mankhwala ophera tizilombo, ects.Veyong imapereka ma API, zokonzekera zolembera zopitilira 100, ndi ntchito za OEM & ODM.

    Veyong (2)

    Veyong amawona kufunikira kwakukulu ku kasamalidwe ka EHS(Environment, Health & Safety) system, ndipo adalandira ziphaso za ISO14001 ndi OHSAS18001.Veyong adalembedwa m'mabizinesi omwe akutuluka m'chigawo cha Hebei ndipo amatha kuonetsetsa kuti zinthu zikuyenda bwino.

    HEBEI VEYONG
    Veyong adakhazikitsa dongosolo lathunthu la kasamalidwe kaubwino, adapeza satifiketi ya ISO9001, satifiketi ya China GMP, satifiketi ya APVMA GMP ya Australia, satifiketi ya GMP ya Ethiopia, satifiketi ya Ivermectin CEP, ndipo idapita ku US FDA.Veyong ali ndi gulu la akatswiri olembetsa, malonda ndi ntchito zaukadaulo, kampani yathu idadalitsidwa ndi chithandizo kuchokera kwamakasitomala ambiri ndi mtundu wabwino kwambiri wazinthu, zogulitsa zapamwamba kwambiri komanso ntchito zotsatsa pambuyo pa malonda, kasamalidwe kakulu ndi sayansi.Veyong wapanga mgwirizano wautali ndi mabizinesi ambiri odziwika padziko lonse lapansi ogulitsa nyama ndi zinthu zomwe zimatumizidwa ku Europe, South America, Middle East, Africa, Asia, etc. mayiko ndi zigawo zopitilira 60.

    VEYONG PHARMA

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