Ceftiofur Sodium Foda don allura

Takaitaccen Bayani:

Babban sashi: Ceftiofur sodium

Ƙayyadaddun bayanai: An ƙidaya bisa ga C1H17N5OS3 (1) 0.1g (2) 0.2g (3) 0.5g (4) 1.0g (5) 4.0g

Dabbobin Target:Shanu, Tumaki, Alade, Kaza

Takaddun shaida:GMP&ISO9001

Sabis:OEM&ODM, mai kyau bayan sabis na tallace-tallace

Rayuwar rayuwa:shekaru 3

 

 


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
shanu awaki tumaki aladu kaji

Cikakken Bayani

Bayanin Kamfanin

Tags samfurin

Pharmacological mataki

PharmacodynamicsCeftiofur magani ne na ƙwayoyin cuta na β-lactam tare da babban tasirin ƙwayoyin cuta kuma yana da tasiri ga ƙwayoyin gram-positive da gram-korau (ciki har da β-lactamase-samuwar ƙwayoyin cuta).Tsarinsa na ƙwayoyin cuta shine ya hana haɗakar bangon ƙwayoyin cuta da kuma haifar da mutuwar kwayan cuta.Wasu Pseudomonas aeruginosa da enterococci suna jure wa miyagun ƙwayoyi.Ayyukan ƙwayoyin cuta na wannan samfurin ya fi na ampicillin ƙarfi, kuma aikinsa na streptococci ya fi ƙarfin na fluoroquinolones.

ceftiofur sodium foda allura

PharmacokineticsIntramuscularly da subcutaneous injections na ceftiofur suna cikin hanzari da kuma rarrabawa, amma ba zai iya shiga shingen kwakwalwar jini ba.Maganin miyagun ƙwayoyi a cikin jini da nama yana da girma, kuma ana kiyaye tasirin magungunan jini mai tasiri na dogon lokaci.Metabolite mai aiki desfuroylceftiofur (Desfuroylceftiofur) za a iya samar da shi a cikin jiki, kuma yana ƙara haɓaka cikin samfuran marasa aiki don fitar da su cikin fitsari da najasa.

Aiki da Amfani

β-Lactam maganin rigakafi.An fi amfani da shi don magance cututtukan ƙwayoyin cuta na dabbobi da kaji.Kamar shanu, ciwon ƙwayar cuta na ƙwayoyin cuta na ƙwayar cuta da kuma kaji Escherichia coli, ciwon Salmonella da sauransu.

Amfani da Dosage

Ceftiofur ne ya ƙididdige shi.Intramuscular allura: kashi daya, 3 ~ 5mg da 1kg nauyin jiki don aladu;sau daya a rana, tsawon kwanaki 3 a jere.Allurar subcutaneous: 0.1 MG kowace tsuntsu don kaji mai kwana 1

Mummunan halayen

(1) Yana iya haifar da tashin hankali flora na gastrointestinal fili ko superinfection.

(2) Yana da wasu nephrotoxicity.

(3) Jin zafi na wucin gadi na gida na iya faruwa.

Matakan kariya

(1) Shirye-shiryen amfani.

(2) Ya kamata a daidaita kashi don dabbobi da rashin wadatar koda.

(3) Mutanen da ke da matuƙar kula da maganin rigakafi na beta-lactam yakamata su guji hulɗa da wannan samfur.

Mu'amalar Magunguna

Yana da tasirin synergistic lokacin amfani da shi tare da penicillin da aminoglycosides.

Lokacin janyewa

Kwanaki 4 don aladu.

Kayayyaki

Wannan samfurin fari ne zuwa foda mai launin ruwan rawaya ko maras kyau

Adana

Inuwa, hana iska, da adanawa a wuri mai sanyi.


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    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.

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