Ingredients: (in the form of amoxicillin trihydrate), gentamicin sulfate and auxiliary substances. A reliable drug based on amoxicillin and gentamicin for the treatment of large and small cattle, horses, camels, pigs, dogs and cats in infectious diseases of the gastrointestinal tract, respiratory tract, genitourinary system, joints, soft tissues and skin, necrobacteriosis, umbilical infections, atrophic rhinitis, metritis-mastitis-agalactia syndrome and other primary and secondary infections of bacterial etiology. The combination of amoxicillin and gentamycin has a broad antibacterial spectrum including gram-positive and gram-negative mycorrhizons (Actynomyces spp., Bacillus antracis, Clostridium spp., Corynebacterium spp., Erysipelothrix rhusiopathiae, Listeria monocytogenes, Staphylococcus spp., Escherichia coli, Haemophilus spp., Pasteurella spp. , Salmonella spp., Streptococcus spp, Actinobacillus spp., Proteus mirabilis, Leptospira spp.). Prolonged action 24 hours. Fast therapeutic effect. Advantageous cost of treatment. 

Ingredients: amoxicillin, clavulanic acid (in the form of calcium clavulanate), excipients. A reliable drug for the treatment of animals based on amoxicillin and clavulanic acid, overcoming resistance to beta-lactam antibiotics. Clavulanic acid inactivates penicillas and, thus, restores the sensitivity of penicillin-resistant microorganisms to the bactericidal action of amoxicillin. Aklatsin is used for cattle, horses, camels, pigs, dogs and cats for respiratory diseases of bacterial etiology, postpartum infections, metrites, mastitis, infections of the skin and soft tissues, necrobacteriosis and other primary and secondary bacterial infections whose pathogens are sensitive to amoxicillin. Prolonged action 24 hours. High therapeutic effectiveness. Advantageous cost of treatment. 

Ingredients: oxytetracycline hydrochloride in the form of magnesium complex and auxiliary substances. The drug is based on the magnesium complex oxytetracycline for the treatment and prophylaxis of respiratory diseases, with pasteurellosis, septicemia, anaplasmosis, hoof rot, for auxiliary therapy with metrites, mastitis, MMA sows syndrome, atrophic rhinitis, erysipelas, wound and postpartum infections, secondary infections in viral diseases and other diseases that are caused by microorganisms sensitive to oxytetracycline hydrochloride. The spectrum of action covers most gram-positive and gram-negative bacteria: streptococci, staphylococci, corynebacteria, clostridia, erysipelotriks, pasterella, salmonella, pseudomonas, hemophilus, actinobacteria, shigella, escherichia, chlamydia, rickettsia, spirochetes and mycoplasma. Prolonged action 48 and 72 hours – treatment course – 1 injection. Advantageous cost of treatment. 

Ingredients:gentamycin sulfate, enrofloxacin and excipients. 

Gentaflox is a highly effective complex preparation of the latest generation with a wide spectrum of antimicrobial action. Enrofloxacin, which is the active ingredient of Gentaflox, inhibits the bacterial DNA of the bacteria, thereby disrupting the DNA replication process, as a result of which microorganisms can not reproduce. Enrofloxacin is rapidly absorbed into the blood and penetrates into all organs and tissues of the body. Gentamicin sulfate, which is part of the drug, is a mixture of several antibiotics produced by Micromonospora purpurea. It has a broad spectrum of antimicrobial activity, is active against most gram-positive and some gram-negative microorganisms, including Staphylococcus spp., Streptococcus spp., Salmonella spp., Proteus mirabilis, Escherichia coli. Antibiotic does not affect anaerobic bacteria, viruses, protozoa and fungi. 

Ingredients: sulfate, oxytetracycline hydrochloride, nystatin, auxiliary and form-building components. Metrobiotic due to the complex of its antimicrobial agents (neomycin sulfate, oxytetracycline hydrochloride and nystatin) has a wide spectrum of antimicrobial activity against pathogens of postnatal infections of genital organs of agricultural animals of bacterial and fungal etiology. Due to the foam-forming basis, the active substances are evenly distributed over the mucous membrane of the uterus. Exposed carbon dioxide enhances the resorption of medicinal substances, promotes penetration of them into the deeper layers of the endometrium. The drug is highly therapeutic and low-cost treatment. 

Ingredients: zinc oxide, chlorhexidine digluconate, and also talc. Antiseptic, dermatoprotective agent. Powder spray forms a protective coating on the skin, heals, disinfects, adsorbs, dries, removes irritation and inflammation, cleanses, increases skin elasticity. Zinc oxide reduces the severity of exudation processes, removes local manifestations of irritation and inflammation, forms a protective coating on the skin that reduces the effect on it of various irritating factors, has an adsorbing and drying effect. Chlorhexidine digluconate disinfects the skin, protects against various microflora. It increases the barrier properties of the skin, accelerates the detoxification of the skin, restores the antioxidant, immune status. Prevents the destruction of elastin when exposed to ultraviolet radiation. Interacting, the components of Powder Spray soothe sensitive or affected skin areas, relieve irritation, provide rapid healing. 

Ingredients: rifampicin, colistin, carbacholin and auxiliary substances. Rikolum is used for the prevention and treatment of inflammation of the uterus of cows after complicated and pathological births, retention of the afterbirth, acute postpartum catarrhal, purulent and chronic endometritis, pyometritis, caesarean section. Rifampicin, which is part of the drug, has a bactericidal effect against many gram-positive, as well as some Gram-negative microorganisms. Colistin is active against gram-negative bacteria: salmonella, shigella, pasteurella, intestinal and pseudomonas aeruginosa, and protozoa and fungi of the genus Candida. Carbacholin increases the tone of the musculature of the uterus. Foaming base of the drug promotes a uniform distribution of active substances on the mucous membrane of the uterus. Exposed carbon dioxide enhances the resorption of medicinal substances, promotes penetration of them into the deeper layers of the endometrium. 

Ingredients: sodium hydroxide, calcium hydroxide and auxiliary substances. Paste “Rognet” – a means to prevent the growth of horns in young cattle and small cattle. Sodium hydroxide and calcium hydroxide, which are part of the product, have a strong local cauterizing effect. When used under the action of alkalis, protein coagulation takes place and the horn growth point is damaged, up to its destruction, which leads to complete cessation of horn growth in young and large cattle. 

Ingredients: zinc, copper in the form of chelated compounds, formic acid, lactic acid, acetic acid, oil eucalyptus, as well as adhesive components and form-building agents. Sangel – a drug for the treatment and prevention of hoof diseases. It has antimicrobial and adhesive properties, accelerates the healing of wounds, abrasions, cracks. It retains its properties after contact with manure and in conditions of high humidity. Copper and zinc, which are part of the gel, have antimicrobial properties. Chelate copper and zinc compounds provide activation of local defense mechanisms and accelerate the healing of wounds, abrasions, cracks, and help maintain moisture. The chelated form of copper and zinc determines high antimicrobial and wound-healing activity, and also provides high resistance to negative effects of unfavorable environmental factors. The gel has good adhesive properties. The properties of the drug persist after contact with manure and in conditions of high humidity. Sangel has a high therapeutic efficiency, while it is cheaper than foreign analogues. Contains eucalyptus oil, which has an additional antiseptic effect, helps to reduce the local irritant effect of other components of the drug (has a “cooling” effect). 

Ingredients: β-carotene, vitamin E (alpha-tocopherol acetate), squalene. Skvartam is a co-ordinated vitamin supernatant. Due to the presence of beta-carotene and vitamin E in its composition, it has a synergistic effect on the animal organism, which is expressed in the normalization of metabolism. prevention of hypo- and avitaminosis A and E, increasing reproductive functions, reducing morbidity and mortality, increasing productivity. β-carotene, which is part of the drug, is a precursor and the main source of vitamin A, not produced in the animal body, and its role in the reproductive sphere is much higher than the actual vitamin A. Vitamin E regulates fat metabolism, stimulates the synthesis of gonadotropic hormones in the pituitary gland, normalizes metabolism in the mucous membrane of the uterus, stimulates the exchange of sulfur-containing amino acids and vitamin C, increases the antioxidant status of the organism. Due to these properties, vitamin E primarily regulates the sexual function of animals and ensures the normal development of the fetus. When vitamin E deficiency is observed, embryo death, decreased fertility due to a disorder of the physiological functions of the uterus, degeneration of testes and sterility in males are noted. Additionally contained in the preparation of vitamin E, derived from plant raw materials – has no analogues in activity among other natural and synthetic forms of this vitamin. Squalene, contained in the preparation, is the precursor of steroids and steroid hormones, as a result of which it has a pronounced positive effect in functional disorders of ovarian hypofunction, uterine subinvolution, ovarian cyst, persistent yellow body in females, and in prevention of sperm quality reduction in males. Squalene is also a precursor of cholesterol – a metabolite that determines growth activity, it also has a positive effect on rickets and osteodystrophy. It is an antioxidant, an activator of growth and promotes an increase in the resistance of the body and the normalization of calcium metabolism. Has the property of inhibiting the replication of viruses. Skvartam is currently unparalleled.

Composition: sulfadiazine, trimethoprim and auxiliary components. Sulfatrimet – a drug for the treatment of cattle, horses, camels, small cattle and pigs in the complex therapy of bacterial infections caused by microorganisms sensitive to the components of the drug, including diseases of the respiratory and genitourinary system, the digestive tract. Complex treatment of postoperative and postpartum complications, infections of the oral cavity (stomatitis, gingivitis) and otitis. It can be used for antibacterial treatment in surgical cases in which there are infections, for example, with an open fracture and in an established peritonitis. Has a wide spectrum of antibacterial action against most Gram-positive and Gram-negative microorganisms, incl. E. coli, Salmonella spp., Staphylococcus spp., Streptococcus spp., Shigella spp. other microorganisms, as well as some protozoa such as Coccidia and Toxoplasma gondi. Sulfadiazine sodium disrupts the synthesis of dihydrofolic acid in bacterial cells, preventing the inclusion of para-aminobenzoic acid in its molecule. Trimethoprim enhances the action of sulfadiazine, disrupting the reduction of dihydrofolic acid into tetrahydrofolic acid, the active form of folic acid, responsible for protein metabolism and division of the microbial cell. With a combined action, the synthesis of folic acid in two consecutive stages is violated, which significantly enhances the bactericidal action of the combination of sulfadiazine and trimethoprim. 

Ingredients: sulfadimethoxin, tetracycline and trimethoprim and auxiliary substances. Trisulfox is intended for treatment of bacterial diseases of cattle, horses, camels, sheep, goats, pigs, dogs, cats, rabbits and poultry (chickens, ducks, geese, turkeys, quails, pigeons), localized in the gastrointestinal tract, respiratory pathways, urogenital system caused by microorganisms sensitive to the combination of sulfadimezin-tetracycline-trimethoprim. Sulfadimethoxin and trimethoprim, which are part of the preparation, individually act on the microbial cell bacteriostatically, and together exhibit synergism of action, ie, enhance the action of each other. The bactericidal action of Trisulfox is due to the sequential blockade of enzymes in the microbial cell: sulfamethazine disrupts the synthesis of dihydrofolic acid, and trimethoprim blocks the next stage of the metabolism of the bacteria – the reduction of dihydrofolic acid into tetrahydrofolic acid, which is necessary for the development of microorganisms. The drug has a wide spectrum of action against gram-negative and gram-positive microorganisms, including Clostridium spp., E. Coli, Salmonella spp., Haemophilus spp., Pasteurella spp, Proteus mirabilis, Streptococcus spp. Antibacterial components of zinaprima are well absorbed from the gastrointestinal tract and quickly distributed to all organs and tissues of the body. Tetracycline hydrochloride is a bacteriostatic antibiotic of the group of tetracyclines of a wide spectrum of action. Acts due to the inhibition of protein synthesis due to blocking the binding of aminoacyl-transport RNA (tRNA) to the “information RNA (mRNA) -bibosome” complex. It is active against Gram-positive (Staphylococcus spp., Including penicillinase-producing Streptococcus spp., Including Streptococcus pneumoniae); Haemophilus influenzae, Listeria spp., Bacillus anthracis) and Gram-negative microorganisms (Neisseria gonorrhoeae, Bordetella pertussis, Escherichia coli, Enterobacter spp., Klebsiella spp., Salmonella spp., Shigella spp.), And Ricketsia spp., Chlamydia spp., Mycoplasma spp., Treponema spp. Resistant to the drug: Pseudomonas aeruginosa, Proteus spp., Serratia spp., Most strains of Bacteroides spp. and fungi, small viruses. Excreted from the body mainly with urine. A scientifically valid combination of antisunrobacterial trisulphoxes makes it extremely effective in the majority of bacterial diseases of different species of animals and birds

Ingredients: Florfenicol and auxiliary substances. Floranite is used to treat cattle, horses, camels, small cattle, pigs, dogs and cats in infectious diseases of the gastrointestinal tract, respiratory tract, genitourinary system, with keratoconjunctivitis of bacterial etiology; diseases of hoofs and other infectious diseases caused by microorganisms sensitive to Florfenicol. Florfenicol, which is a synthetic broad-spectrum antibiotic of the amphenicol group, is a thiamphenicol derivative in which the hydroxyl group is replaced by a fluorine atom. Bactericidal against most Gram-negative and Gram-positive microorganisms, including Staphylococcus spp., Streptococcus spp., Enterobacter spp., Escherichia coli, Pasteurella haemolytica, Pasteurella multocida, Haemophilus somnus, Fusobacterium necrophorum, Bacteroides melaninogenicus, A. pleuropneumoniae, P. multocida , Haemophilus parasuis. Streptococcus suis, Bordetella bronchiseptica, Salmonella spp., Klebsiella spp., Proteus spp., Shigella spp., Moraxella bovis and others. Florfenicol is active against most mycoplasmas (Mycoplasma hyopneumoniae and Mycoplasma hyorhinis and others), as well as against bacteria that produce acetyltransferase and are resistant to chloramphenicol. Florfenicol, binding in the protoplasm of the bacterial cell with the ribosomal subunit of 70S, blocks the enzyme peptidyl transferase, which leads to inhibition of protein synthesis at the level of ribosomes in sensitive microorganisms. After parenteral administration of the drug, florfenicol is rapidly absorbed and penetrates most organs and tissues, reaching maximum serum concentrations in 30-90 minutes, and remains in the body in a therapeutic concentration of at least 48 hours. Retards the growth of some microorganisms (Pasteurella multocida) within 72 hours. The antibiotic is excreted from the body in unmodified form and in the form of metabolites mainly with urine, to a lesser extent with feces. Prolonged action – 48 hours. 

Composition: florfenicol, oxytetracycline hydrochloride, sulfadimezin, nystatin, carbacholin and auxiliary substances. Eridon is used to treat and prevent septic processes of the vulva, vagina, cervix (vulvitis, cervicitis, salpingitis, metritis) in large and small cattle, pigs, horses. All cases of delayed afterbirth. For postpartum infection prevention. Eridon has a broad spectrum of antimicrobial activity, is active against gram-positive and gram-negative bacteria. The drug administered to the animal at recommended doses suppresses the development of pasterella, salmonella, escherichia, cocci, brucella, klebsiella, proteas, yersinia, franciella, mycoplasmas, rickettsia, spirochetes, actinomycetes, chlamydia; fungi of the genus Aspergillus, Candida. Due to the large volume of foam and its stability, the drug envelops and contacts the entire cavity of the animal. Exposed carbon dioxide enhances the resorption of medicinal substances, facilitates penetration of them into the deep layers of the endometrium.

Composition: cloprostenol and auxiliary substances. Estrophan (an analog of Estrofan) is used to regulate the reproductive function and treatment of its pathologies in female farm animals, including: induction of sexual hunting in cows, mares, camels, induction of farrowing in sows; treatment of cows, mares and camels with various forms of ovarian dysfunction: persistent yellow body, follicular (in combination with chorionic or luteinizing hormones) and luteal cysts, ovarian hypofunction (in combination with gonadotropin releasing hormone, follicle stimulating hormone or gonadotropin medications of stallion mares) , prevention and treatment of postpartum diseases of the uterus. To terminate pregnancy in fetal pathologies.

Ingredients: ivermectin, clozantel and auxiliary substances. Cloverin possesses a wide spectrum of antiparasitic action, it is effective against nematodes of the gastrointestinal tract and lungs, trematodes, larvae of gadflies and ectoparasites. The mechanism of action of clozantel, one of the active substances of the preparation, consists in the violation of the processes of phosphorylation and electron transfer, which leads to a violation of the energy exchange and death of the parasite. Ivermectin, another component of the drug, enhances the production of the neurotransmitter inhibition-gamma-aminobutyric acid, blocking the passage of nerve impulses in parasites, which causes paralysis and death of the parasite. After parenteral administration, the active substances of Santomectin are well absorbed from the injection site and penetrate most of the organs and tissues of the body. The therapeutic concentration of the drug persists for 10-12 days. In recommended doses, the drug does not have a mutagenic, sensitizing, embryotoxic and teratogenic effect. It is excreted from the body with urine, bile, feces, in lactating animals – partly with milk.