ผู้ผลิตสัตวแพทยศาสตร์ GMP สำหรับการฉีดน้ำบราฟอะคูล 5 % สำหรับสัตว์ ซู

• ความหลากหลาย: เวชศาสตร์ป้องกันโรคปรสิต
• คอมโพเนนต์: ยาสังเคราะห์ทางเคมี
• พิมพ์: ชั้นหนึ่ง
• ปัจจัยที่มีอิทธิพลต่อการติดตามของเภสัชภัณฑ์: ใช้ร่วมกันไม่ได้
• วิธีการจัดเก็บ: Protected From Light and High Temperature
• การรักษาสัตวแพทย์ ไม่ได้: Na
• ไม่ใช่ ของรุ่น: injection
• GMP: ใช่
• โรงงาน: ใช่
• ตัวอย่าง: ใช่
• แพคเพจการขนส่ง: 120boxes/Carton
• ข้อมูลจำเพาะ: 50ml/vial/box, 120boxes/carton
• เครื่องหมายการค้า: VEYONG
• ที่มา: China
• รหัสพิกัดศุลกากร: 300420
• กำลังการผลิต: 3000L/Day

คำอธิบายสินค้า

 

Specification	5%	Usage	Antibiotic
Raw Material	Buparvaquone	Species	Cattle, sheep, swine, camels,chicken
Dosage Form	injection	Sample	Yes
Packing	100ml/vial/box, 80boxes/carton 50ml/vial/box, 120boxes/carton 10ml/vial/box, 400boxes/carton	Delivery Time	15-20days
MOQ	500L	Payment Term	T/T, D/P, D/A, L/C
GMP	Yes	ISO9001	Yes
FDA	Yes	COS	Yes

 

Product Description

Composition: Contains per ml:
Buparvaquone           50 mg.
Description:
Buparvaquone is a second-generation hydroxynaphtaquinone with novel features that make it an effective compound for the therapy and prophylaxis of all forms of theileriosis.
Indications:
For treatment of tick-transmitted theileriosis caused by the intracellular protozoan parasites Theileria parva (East Coast fever, Corridor disease, Zimbabwean theileriosis) and T. annulata (tropical theileriosis) in cattle. It is active against both the schizont and piroplasm stages of Theileria spp., and may be used during the incubation period of the disease, or when clinical signs are apparent.

 

Contra indications:
Due to the inhibiting effects of theileriosis on the immune system, vaccination should be delayed until the animal has recovered from theileriosis.
Side effects:
Localised, painless, oedematous swelling may occasionally be seen at the injection site.
Dosage:
For intramuscular injection.
The general dosage is 1 ml per 20 kg body weight
In severe cases the treatment may be repeated within 48-72 hours.
Do not administer more than 10 ml per injection site.
Successive injections should be administered at different sites.
Withdrawal times:

For Meat: 42 days, 

For milk: 2 days.

 

Company Profile

Hebei Veyong pharmaceutical Co., Ltd., was established in 2002, located in Shijiazhuang City Hebei Province, China, near the Capital Beijing. It's a large GMP-certified veterinary druo enterprise, with R&D, production and sales of veterinary APlspreparations premixed feeds and feed additives. As Provincial Technical CenterVeyong has established an innovated R&D system for new veterinary drug, and is the nationally knowntechnological innovation-based veterinary enterprise. Veyong has two production bases: Shijiazhuang and Ordos, with 7APl production lines including lvermectin, Eprinomectin, Tiamulin Fumarateects and 12 preparation production lines including injection, oral solution, powder, premix, bolus, pesticides and disinfectant ect. Veyong provides APls, more than 100 own-label preparations and OEM & ODM service.

Vevong established the comolete auality manaement svstem, obtained the ISO9001 certificate, China GMP certificate, Australia APVMA GMP certificate, Ethiopia GMP certificate, Ivermectin CEP certificate, and passed US FDA inspection. Veyong has professional team of registeration, sales and technica service, has made long term cooperation with many internationally known animal pharmaceutical enterprises with products exported to the Europe, South America, Middle East, Africa, Asia, etc. more than 60 countries and regions.
Veyong attaches great importance to the management of EHS (Environment Health & Safety) system, and obtained the lSO14001 and OHSAS18001 certificates. Veyong ha been listed in the strategic emerging industrial enterprises in Hebei Province and can ensure the continuous supply ofproducts.
Vevong takes "Maintain animal health, improve quality of life"as the mission, strives to become the most valuable veterinary drug brand, and looks forward to active cooperation with global customers.

 

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