50% Oxytetracycline Hydrochloride Soluble Powder fun Awọn adiye
Awọn ohun-ini
50% Oxytetracycline hydrochloride tiotuka lulú jẹ ina ofeefee lulú
Pharmacological ipa
Oxytetracycline hydrochloridetiotuka lulú jẹ ti awọn egboogi tetracycline.Oxytetracycline reversibly sopọ si olugba lori 30S subunit ti kokoro ribosome, dabaru pẹlu awọn Ibiyi ti ribosomal eka laarin tRNA ati mRNA, idilọwọ peptide pq elongation ati ki o dojuti amuaradagba kolaginni, nitorina ni kiakia idilọwọ awọn idagbasoke ati atunse ti kokoro arun.Oxytetracycline ṣe idiwọ mejeeji Gram-positive ati Gram-negative kokoro arun.Awọn kokoro arun ni resistance-resistance si oxytetracycline ati doxycycline.
Itọkasi
O ni ipa ti o lagbara lori awọn kokoro arun ti o ni giramu gẹgẹbi Staphylococcus, Streptococcus hemolyticus, Bacillus anthracis, Clostridium tetani ati Clostridium;odi fun awọn kokoro arun Giramu-odi gẹgẹbi Escherichia coli, Salmonella, Brucella ati Pasteurella Bacteria jẹ ifarabalẹ diẹ sii.Ọja yii tun ni ipa inhibitory lori rickettsia, chlamydia, mycoplasma, spirochetes, actinomycetes ati awọn protozoa kan.
Lilo
50% Oxytetracycline hydrochloride tiotuka lulúti wa ni lo lati toju àkóràn arun to šẹlẹ nipasẹ kókó Escherichia coli, Salmonella, Pasteurella ati Mycoplasma ni elede ati adie.
Isakoso ati doseji
Da lori ọja yi.
Adalu omi mimu: fun 1L ti omi, 200-400mg fun elede;300-500mg fun awọn adie.
Lo fun awọn ọjọ 3-5.
Àwọn ìṣọ́ra
(1) 50% Oxytetracycline hydrochloride soluble lulú ko yẹ ki o ni idapo pẹlu awọn oogun penicillin ati awọn oogun tabi awọn ifunni ti o ni iyọ kalisiomu, iyọ irin ati awọn ions irin polyvalent.
(2) Ijọṣepọ pẹlu awọn diuretics ti o lagbara le mu ibajẹ kidirin buru si.
(3) Ọja yii ko dara lati dapọ pẹlu omi tẹ ni kia kia ati ojutu ipilẹ pẹlu akoonu chlorine giga.
(4) Awọn ẹranko alaabo pẹlu ẹdọ ati iṣẹ kidinrin ti ko lagbara pupọ.
Awọn aati buburu
Ohun elo igba pipẹ le fa ipalara meji ati ibajẹ ẹdọ.
Akoko yiyọ kuro
7 ọjọ fun elede ati 5 ọjọ fun adie;
2 ọjọ fun ẹyin abandonment akoko.
Sipesifikesonu
50% iṣiro ni ibamu si C22H24N2O9
Ibi ipamọ Ipo
O yẹ ki o wa ni ipamọ shading, airtight, gbẹ ibi.
Iṣakojọpọ
100g/apo, 500g/apo, 1kg/apo
Hebei Veyong elegbogi Co., Ltd, ti iṣeto ni 2002, be ni Shijiazhuang City, Hebei Province, China, tókàn si awọn Olu Beijing.O jẹ ile-iṣẹ oogun oogun ti ogbo ti GMP nla kan, pẹlu R&D, iṣelọpọ ati tita awọn API ti ogbo, awọn igbaradi, awọn ifunni iṣaaju ati awọn afikun ifunni.Gẹgẹbi Ile-iṣẹ Imọ-ẹrọ Agbegbe, Veyong ti ṣe agbekalẹ eto R&D imotuntun fun oogun oogun titun, ati pe o jẹ ile-iṣẹ ĭdàsĭlẹ imọ-ẹrọ ti a mọ ni orilẹ-ede ti o da lori ile-iṣẹ ti ogbo, awọn alamọdaju imọ-ẹrọ 65 wa.Veyong ni awọn ipilẹ iṣelọpọ meji: Shijiazhuang ati Ordos, eyiti ipilẹ Shijiazhuang ni wiwa agbegbe ti 78,706 m2, pẹlu awọn ọja API 13 pẹlu Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, ati awọn laini iṣelọpọ igbaradi 11 pẹlu abẹrẹ, ojutu oral, , premix, bolus, ipakokoropaeku ati disinfectant, ects.Veyong n pese awọn API, diẹ sii ju awọn igbaradi aami-ara 100, ati iṣẹ OEM & ODM.
Veyong ṣe pataki pataki si iṣakoso ti eto EHS (Ayika, Ilera & Aabo), ati gba awọn iwe-ẹri ISO14001 ati OHSAS18001.A ti ṣe atokọ Veyong ni awọn ile-iṣẹ ile-iṣẹ ti n yọju ilana ni Agbegbe Hebei ati pe o le rii daju ipese awọn ọja nigbagbogbo.
Veyong ṣe agbekalẹ eto iṣakoso didara pipe, gba ijẹrisi ISO9001, ijẹrisi GMP China, ijẹrisi APVMA GMP Australia, ijẹrisi GMP Ethiopia, ijẹrisi Ivermectin CEP, ati pe o kọja ayewo US FDA.Veyong ni ẹgbẹ alamọdaju ti iforukọsilẹ, tita ati iṣẹ imọ-ẹrọ, ile-iṣẹ wa ti ni igbẹkẹle ati atilẹyin lati ọdọ awọn alabara lọpọlọpọ nipasẹ didara ọja ti o dara julọ, awọn tita iṣaaju-didara ati iṣẹ lẹhin-tita, pataki ati iṣakoso imọ-jinlẹ.Veyong ti ṣe ifowosowopo igba pipẹ pẹlu ọpọlọpọ awọn ile-iṣẹ elegbogi ẹranko ti a mọ ni kariaye pẹlu awọn ọja okeere si Yuroopu, South America, Aarin Ila-oorun, Afirika, Esia, ati bẹbẹ lọ ju awọn orilẹ-ede ati agbegbe 60 lọ.