20% Sulfadiazine+4% Trimethoprim Jekiseni

Tsanangudzo Pfupi

Zvinyorwa:

Sulfadiazine 20% w/v;Trimethoprim 4% w/v

Packing:50ml, 100ml

Chitupa:GMP uye ISO

Muenzaniso:Available

Sevhisi:OEM & ODM, yakanaka mushure-sevhisi

 

 


Mutengo weFOB US $0.5 - 9,999 / Piece
Min.Order Quantity 1 Piece/Zvimedu
Supply Ability 10000 Piece / Zvimedu pamwedzi
Nguva yekubhadhara T/T, D/P, D/A, L/C
ngamera mombe mbudzi nguruve hwai

Product Detail

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Active Ingredient

Sulfadiazine 20.00% w/v.

Trimethoprim 4.00% w/v

Pharmacological chiito

Sulfadiazine mushonga wesarufa unoshanda zvine mwero wekushandisa systemic uye ibroad-spectrum bacteriostatic agent.Nzira yaro yekuita imhaka yekuti yakarongeka yakafanana nep-aminobenzoic acid (PABA) uye inogona kukwikwidzana nePABA kuti iite pane dihydrofolate synthase mumabhakitiriya, nokudaro kudzivirira PABA kubva kushandiswa sechinhu chakasvibiswa kugadzira tetrahydrofolate inodiwa nebhakitiriya, nokudaro. inhibiting The synthesis yebacterial protein inotamba antibacterial effect.

sulfadiazine+trimethoprim inj-1

Indlcation

Iyi Injectable Solution inoratidzwa mukurapa kwehutachiona hwehutachiona hunokonzerwa kana hunobatanidza nezvisikwa zvinonzwisisika kune Trimethoprim: Sulfadiazine kusanganiswa.Kuwanda kwekuita kunosanganisira zvese zvipenyu zveGram-positive uye Gram-negative zvinosanganisira: Actinobacilli, Actinomycae, Bordetella spp, Brucella Corynebacteria, Escherichia coli, Haemophilus spp.Klebsiella spp, Pasteurella spp, Pneumococci.Proteus, Salmonella spp.Staphylococci, Streptococci, Vibrio.

Dosage uye kutonga

Ne subcutaneous jekiseni chete.

Mombe: Chiyero chinokurudzirwa i15 mg yezvinwiwa zvinoshanda pakg yehuremu hwemuviri (1 ml pa16kg yehuremu hwemuviri) nejekiseni remuscular or slow intravenous.

Mabhiza: Chiyero chinokurudzirwa i15 mg yezvishandiso zvinoshanda pakg uremu hwemuviri (1 ml pa16 kg uremu hwemuviri), nekunonoka jekiseni remutsinga.

Imbwa neKatsi: Chiyero chinokurudzirwa chiyero ndeye 30mg yezvinhu zvinoshanda pakg uremu hwemuviri (1 ml pa8 kg uremu hwemuviri).

Contraindications

Jekiseni harifanirwe kupihwa neimwe nzira kunze kweinokurudzirwa.

Haifanirwe kupihwa intraperitoneally, intra-arterial kana intrathecally.

Usapire kumhuka dzinozivikanwa sulfonamide senitivity, yakaipisisa chiropa parenchymal kukuvara kana ropa dyscrasias.

Yambiro Yakakosha

1 Pakuisa mutsinga chigadzirwa chinofanirwa kudziirwa kusvika pakupisa kwemuviri uye kubaiwa zvishoma nezvishoma kwenguva yakareba sezvinobvira.

2 Pachiratidzo chekutanga chekusashivirira jekiseni rinofanira kukanganiswa uye kurapwa kwekuvhunduka kutangwa.

Mvura yakakwana yekunwa inofanira kuwanikwa panguva yekurapa kwechigadzirwa.

Withdrawal Period

Mombe : Nyama - mazuva gumi nemaviri

Mukaka - 4 mazuva.

Storage

Dzivirira kubva kuzuva rakananga uye chengetedza pasi pe30 ℃.


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

    Hebei Veyong Pharmaceutical Co., Ltd, yakavambwa muna 2002, iri muShijiazhuang City, Hebei Province, China, padyo neguta guru Beijing.Iye ihombe GMP-yakasimbiswa veterinary drug bhizinesi, ine R&D, kugadzira uye kutengesa kweVeterinary APIs, gadziriro, premixed feed uye feed additives.SeProvincial Technical Center, Veyong yakamisa hurongwa hweR&D hwemishonga mitsva yezvipfuyo, uye ndiyo inozivikanwa pasi rose tekinoroji innovation yakavakirwa bhizinesi rezvipfuyo, kune makumi matanhatu neshanu nyanzvi.Veyong ine mabhesi maviri ekugadzira: Shijiazhuang neOrdos, iyo iyo Shijiazhuang base inovhara nzvimbo ye78,706 m2, ine 13 API zvigadzirwa zvinosanganisira Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, uye 11, gadziriro yekugadzira oral poda, mitsara yekugadzira oral. , premix, bolus, mishonga yezvipembenene nemishonga inouraya utachiona, ects.Veyong inopa APIs, anopfuura zana ega- label gadziriro, uye OEM & ODM sevhisi.

    Veyong (2)

    Veyong inokoshesa zvikuru manejimendi eEHS(Environment, Health & Safety) system, uye yakawana ISO14001 uye OHSAS18001 zvitupa.Veyong yakanyorwa mumabhizinesi ari kusimukira maindasitiri muHebei Province uye inogona kuve nechokwadi chekuenderera mberi kwezvigadzirwa.

    HEBEI VEYONG
    Veyong yakamisa hurongwa hwekutonga kwemhando yakakwana, yakawana chitupa cheISO9001, chitupa cheChina GMP, chitupa cheAustralia APVMA GMP, chitupa cheEthiopia GMP, chitupa cheIvermectin CEP, uye yakapasa ongororo yeUS FDA.Veyong ine timu yehunyanzvi yekunyoresa, kutengesa uye tekinoroji sevhisi, kambani yedu yakawana kuvimba nerutsigiro kubva kune akawanda vatengi nemhando yepamusoro yechigadzirwa, yepamusoro-yemhando yepamusoro-yekutanga kutengesa uye mushure mekutengesa sevhisi, yakakomba uye yesainzi manejimendi.Veyong yaita kushandira pamwe kwenguva refu nemabhizinesi mazhinji anozivikanwa pasi rose emishonga yemhuka ane zvigadzirwa zvinotengeswa kuEurope, South America, Middle East, Africa, Asia, etc. kupfuura nyika makumi matanhatu nematunhu.

    VEYONG PHARMA

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