25% Tilmicosin Oral Solution for chicken
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Composition
100ml contains 25g Tilmicosin.
Pharmacological action
Pharmacodynamics Teicoplanin is a semisynthetic macrolide antibiotic dedicated to animals. For mycoplasma, the antibacterial effect is similar to that of tylosin, and the sensitive gram-positive bacteria are Staphylococcus aureus (including penicillin-resistant Staphylococcus aureus), pneumococcus, streptococcus, Bacillus anthracis, Erysipelothrix rhusiopathiae, Listeria monocytogenes, Portunus putrefaciens, and Portunus emphysematosus. Sensitive gram-negative bacteria include Haemophilus, meningococcus and Pasteurella. It is more active than tylosin against Actinobacillus pleuropneumoniae, Pasteurella and Mycoplasma bovis. Ninety-five percent of Pasteurella haemolytica strains are susceptible to this product.
Pharmacokinetics
Tilmicosin solution is rapidly absorbed after oral administration and is characterized by strong tissue penetration and large volume of distribution (greater than 2 L/kg). The concentration in the lung is high, the elimination half-life can reach 1 to 2 days, and the effective plasma concentration is maintained for a long time.
Drug interactions
(1) Tilmicosin has the same target as other macrolides and lincosamines and should not be used at the same time.
(2) the combination with β-lactams showed antagonism.
Withdrawal Time
27days before slaughter.
Not for use in dairy cattle of breeding age, or in any cattle during the first 45 days of pregnancy (or first 45 days after removing bull)
Action and use
Macrolide antibiotics. Used for treatment of chicken respiratory diseases caused by Pasteurella and Mycoplasma.
Dosage and administration
Mixed drink: 0.3 ml per 1 L of water for chickens. For 3 days.
Adverse reactions
The toxic effect of this product on animals is mainly cardiovascular system, which can cause tachycardia and weakened contractility
Precautions
Tilmicosin oral solution is contraindicated in laying hens during the laying period.
Withdrawal Period
Chickens for 12 days.
Storage
Store in sealed condition, protected from light.
Hebei Veyong pharmaceutical Co., Ltd, was established in 2002, located in Shijiazhuang City, Hebei Province, China, next to the Capital Beijing. She is a large GMP-certified veterinary drug enterprise, with R&D, production and sales of veterinary APIs, preparations, premixed feeds and feed additives. As Provincial Technical Center, Veyong has established an innovated R&D system for new veterinary drug, and is the nationally known technological innovation based veterinary enterprise, there are 65 technical professionals. Veyong has two production bases: Shijiazhuang and Ordos, of which the Shijiazhuang base covers an area of 78,706 m2, with 13 API products including Ivermectin, Eprinomectin, Tiamulin Fumarate, Oxytetracycline hydrochloride ects, and 11 preparation production lines including injection, oral solution, powder, premix, bolus, pesticides and disinfectant, ects. Veyong provides APIs, more than 100 own- label preparations, and OEM & ODM service.
Veyong attaches great importance to the management of EHS(Environment, Health& Safety) system, and obtained the ISO14001 and OHSAS18001 certificates. Veyong has been listed in the strategic emerging industrial enterprises in Hebei Province and can ensure the continuous supply of products.
Veyong established the complete quality management system, 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 technical service, our company has gained reliance and support from numerous customers by excellent product quality, high-quality pre-sales and after-sales service, serious and scientific management. Veyong 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.
