| Suspension for oral administration. | ||||||||||||
| Composition: | ||||||||||||
Contains per ml.:
| ||||||||||||
| Description: | ||||||||||||
| Albendazole is a synthetic anthelmintic which belongs to the group of benzimidazole-derivatives with activity against a broad range of worms and at a higher dosage level also against adult stages of liver‑fluke. | ||||||||||||
| Indications: | ||||||||||||
Prophylaxis and treatment of worminfections in calves, cattle, goats and sheep like:
| ||||||||||||
| Contra indications: | ||||||||||||
| Administration in the first 45 days of gestation.
| ||||||||||||
| Side effects: | ||||||||||||
| - Hypersensitivity reactions.
| ||||||||||||
| Dosage: | ||||||||||||
For oral administration:
Shake well before use. | ||||||||||||
| Withdrawal times: | ||||||||||||
| ||||||||||||
| Warning: | ||||||||||||
| Keep out of reach of children. | ||||||||||||
| Packing: | ||||||||||||
| Bottle containing 100 ml. and Jerrycan of 500 and 1000 ml.
| ||||||||||||
| Form of product | : Oral liquids |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Albendazole |
| Suspension for oral administration. | ||||||||||||
| Composition: | ||||||||||||
| ||||||||||||
| Description: | ||||||||||||
| Albendazole is a synthetic anthelmintic, which belongs to the group of benzimidazole-derivatives with activity against a broad range of worms and at a higher dosage level also against adult stages of liver fluke. | ||||||||||||
| Indications: | ||||||||||||
Prophylaxis and treatment of worminfections in calves, cattle, goats and sheep like:
| ||||||||||||
| Contra indications: | ||||||||||||
| Administration in the first 45 days of gestation. | ||||||||||||
| Side effects: | ||||||||||||
| Hypersensitivity reactions. | ||||||||||||
| Dosage: | ||||||||||||
For oral administration:
Shake well before use. | ||||||||||||
| Withdrawal times: | ||||||||||||
| ||||||||||||
| Warning: | ||||||||||||
| Keep out of reach of children. | ||||||||||||
| Packing: | ||||||||||||
| Bottle containing 100 ml. and Jerrycan of 500 and 1000 ml. | ||||||||||||
| Form of product | : Oral liquids |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Albendazole |
| Bolus for oral administration. | |||||||||||||
| Composition: | |||||||||||||
Contains per bolus.:
| |||||||||||||
| Description: | |||||||||||||
| Albendazole is a synthetic anthelmintic which belongs to the group of benzimidazole-derivatives with activity against a broad range of worms and at a higher dosage level also against adult stages of liver fluke. | |||||||||||||
| Indications: | |||||||||||||
Prophylaxis and treatment of worminfections in calves and cattle like:
| |||||||||||||
| Contra indications: | |||||||||||||
| Administration in the first 45 days of gestation. | |||||||||||||
| Side effects: | |||||||||||||
| Hypersensitivity reactions. | |||||||||||||
| Dosage: | |||||||||||||
For oral administration.
| |||||||||||||
| Withdrawal times: | |||||||||||||
| |||||||||||||
| Warning: | |||||||||||||
| Keep out of reach of children. | |||||||||||||
| Packing: | |||||||||||||
| 50 boluses in a carton with blister. | |||||||||||||
| Form of product | : Bolus |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Albendazole |
| Bolus for oral administration. | ||||||||||||
| Composition: | ||||||||||||
Contains per bolus.:
| ||||||||||||
| Description: | ||||||||||||
| Albendazole is a synthetic anthelmintic which belongs to the group of benzimidazole-derivatives with activity against a broad range of worms and at a higher dosage level also against adult stages of liver fluke.
| ||||||||||||
| Indications: | ||||||||||||
Prophylaxis and treatment of worminfections in cattle, calves, sheep and goats like:
| ||||||||||||
| Contra indications: | ||||||||||||
| Administration in the first 45 days of gestation. | ||||||||||||
| Side effects: | ||||||||||||
| Hypersensitivity reactions. | ||||||||||||
| Dosage: | ||||||||||||
For oral administration.
| ||||||||||||
| Withdrawal times: | ||||||||||||
| ||||||||||||
| Warning: | ||||||||||||
| Keep out of reach of children. | ||||||||||||
| Packing: | ||||||||||||
| 50 boluses in a carton with blister. | ||||||||||||
| Form of product | : Bolus |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Albendazole |
| Bolus for oral administration. | ||||||||||||
| Composition: | ||||||||||||
Contains per bolus.:
| ||||||||||||
| Description: | ||||||||||||
| Albendazole is a synthetic anthelmintic which belongs to the group of benzimidazole-derivatives with activity against a broad range of worms and at a higher dosage level also against adult stages of liver fluke. | ||||||||||||
| Indications: | ||||||||||||
Prophylaxis and treatment of worminfections in calves, cattle, sheep and goats like:
| ||||||||||||
| Contra indications: | ||||||||||||
| Administration in the first 45 days of gestation. | ||||||||||||
| Side effects: | ||||||||||||
| Hypersensitivity reactions. | ||||||||||||
| Dosage: | ||||||||||||
For oral administration.
| ||||||||||||
| Withdrawal times: | ||||||||||||
| ||||||||||||
| Warning: | ||||||||||||
| Keep out of reach of children. | ||||||||||||
| Packing: | ||||||||||||
| 50 boluses in a carton with blister. | ||||||||||||
| Form of product | : Bolus |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Albendazole |
| Fast Desinfectant for Surfaces | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| Description: | ||||||
| Alcodex is used for fast disinfection of surfaces of medical devices. The substance is a ready-made solution, it does not contain glutamic aldehyde. Upon spraying, the solution covers surfaces evenly, it does not leave any spots upon drying. Suitable for using on all alcohol-enduring surfaces. Alcodex has a wide fungicidal and bactericidal effect, destroys Gram-positive and Gram-negative bacteria (including the generator of tuberculosis), deactivates viruses (HBV, HIV, Rota). pH: 6,5-7,5 | ||||||
| Indications: | ||||||
| Alcodex is used as a concentrate for disinfection of alcohol-enduring surfaces. If endurance of a surface is not known, it can be tested on an inconspicuous spot of the surface. It is not suitable for using on acryl glass and alcohol-solved varnish. The preparation is sprayed on the surface and wiped over it. The surfaces have to be covered in full. The time of effect is 1-3 minutes. | ||||||
| Withdrawal times: | ||||||
| None. | ||||||
| Warning: | ||||||
| Keep away from sources of ignition
In case of contact with eyes, rinse immidiately with plenty of water and seek medical advice. | ||||||
| Packing: | ||||||
| 5 litre can. | ||||||
| Form of product | : Disinfectants |
| Type of product | : Disinfectants |
| Suited for animals | : Camels |
| Active ingredients | : Quaternary ammonium compounds |
| Powder for oral administration. | ||||||||||||||||||||||||||||||||||
| Composition: | ||||||||||||||||||||||||||||||||||
Contains per gram powder:
| ||||||||||||||||||||||||||||||||||
| Description: | ||||||||||||||||||||||||||||||||||
| Highly effective combination of broad-spectrum antibiotics and vitamins.
Colistin is an antibiotic from the group of polymyxins with a bactericidal action against Gram-negative bacteria like E. coli, Haemophilus and Salmonella. Since colistin is absorbed for a very small part after oral administration only gastrointestinal indications are relevant. Oxytetracycline belongs to the group of tetracyclines and acts bacteriostatic against many Gram-positive and Gram-negative bacteria like Bordetella, Campylobacter, Chlamydia, E. coli, Haemophilus, Mycoplasma, Pasteurella, Rickettsia, Salmonella, Staphylococcus and Streptococcus spp. The action of oxytetracycline is based on inhibition of bacterial protein synthesis. Oxytetracycline is mainly excreted in urine, for a small part in bile and in lactating animals in milk. Erythromycin is a macrolide that acts bacteriostatic against mainly Gram-positive bacteria like Mycoplasma, Staphylococcus and Streptococcus spp. Streptomycin is an aminoglycoside with a bactericidal action against mainly Gram-negative bacteria like E. coli, Klebsiella, Pasteurella, Salmonella and Staphylococcus spp. Vitamins are essential for the proper operation of several physiological functions. | ||||||||||||||||||||||||||||||||||
| Indications: | ||||||||||||||||||||||||||||||||||
| Aliseryl WS is a highly effective combination of broad-spectrum antibiotics and vitamins. The product stimulates egg production, increases growth, improves feed conversion and used as vitamin supplement during periods of diseases and stress. Gastrointestinal, respiratory and urinary infections caused by colistin, oxytetracyclin, erythromycin and streptomycin sensitive micro-organisms, like Bordetella, Campylobacter, Chlamydia, E. coli, Haemophilus, Klebsiella, Mycoplasma, Pasteurella, Rickettsia, Salmonella, Staphylococcus and Streptococcus spp. in calves, goats, sheep, poultry and swine. | ||||||||||||||||||||||||||||||||||
| Contra indications: | ||||||||||||||||||||||||||||||||||
| Hypersensitivity to tetracyclines, macrolides, colistin or aminoglycocides.
Administration to animals with a serious impaired renal and/or liver function. Concurrent administration with penicillines, cephalosporines, quinolones and cycloserine. Administration to animals with an active microbiological digestion. | ||||||||||||||||||||||||||||||||||
| Side effects: | ||||||||||||||||||||||||||||||||||
| No undesirable effects are to be expected when the prescribed dosage regimen is followed. | ||||||||||||||||||||||||||||||||||
| Dosage: | ||||||||||||||||||||||||||||||||||
| For oral administration.
Poultry and swine:
Note: for pre-ruminant calves, lambs and kids only. | ||||||||||||||||||||||||||||||||||
| Withdrawal times: | ||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||
| Warning: | ||||||||||||||||||||||||||||||||||
| Keep out of reach of children. | ||||||||||||||||||||||||||||||||||
| Packing: | ||||||||||||||||||||||||||||||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | ||||||||||||||||||||||||||||||||||
| Form of product | : Water soluble powders |
| Type of product | : Growth stimulators,Vitamins,Antibiotics (Non penicillins),Amino Acids |
| Suited for animals | : Goats,Sheep,Calves |
| Active ingredients | : Colistin sulphate,Erythromycin thiocyanate,Oxytetracycline.HCl,Vitamins |
| Insecticide for external use | ||||||||||||||||||||||||||||
| Composition: | ||||||||||||||||||||||||||||
Contains per ml.:
| ||||||||||||||||||||||||||||
| Indications: | ||||||||||||||||||||||||||||
| Used to control of susceptible lice on unshorn sheep and lambs with up to 10 months wool.
Rain before or after treatment has little effect on product performance. | ||||||||||||||||||||||||||||
| Dosage: | ||||||||||||||||||||||||||||
Dosage rate for lice control:
* Note: months of wool growth assumes flat comb shearing. Fly control:
| ||||||||||||||||||||||||||||
| Withdrawal times: | ||||||||||||||||||||||||||||
| Meat: 7 days
Animals producing meat or offal for human consumption must not be sold for slaughter either during treatment or within seven days of cessation of the last treatment. Milk: 35 days Milk intended for sale for human consumption must be discarded during treatment and for not less than 35 days following the last treatment. | ||||||||||||||||||||||||||||
| Warning: | ||||||||||||||||||||||||||||
| Keep out of reach of children. | ||||||||||||||||||||||||||||
| Packing: | ||||||||||||||||||||||||||||
| Plastic bottle of 100 and 1000 ml. | ||||||||||||||||||||||||||||
| Form of product | : Pesticides |
| Type of product | : Pesticides |
| Suited for animals | : Sheep,Lambs |
| Active ingredients | : Alpha-cypermethrin |
| Solution for oral administration. | ||||||||||||||||||||||||||||||||||||||
| Composition: | ||||||||||||||||||||||||||||||||||||||
Contains per ml.:
| ||||||||||||||||||||||||||||||||||||||
| Description: | ||||||||||||||||||||||||||||||||||||||
| Amino acids are essential for the proper operation of several physiological functions.
Amino acids are from non animal origin. | ||||||||||||||||||||||||||||||||||||||
| Indications: | ||||||||||||||||||||||||||||||||||||||
Aminogrow Oral is a well balanced combination of essential amino acids for calves, cattle, goats, poultry, sheep and swine. Aminogrow Oral is used for:
| ||||||||||||||||||||||||||||||||||||||
| Side effects: | ||||||||||||||||||||||||||||||||||||||
| No undesirable effects are to be expected when the prescribed dosage regimen is followed. | ||||||||||||||||||||||||||||||||||||||
| Dosage: | ||||||||||||||||||||||||||||||||||||||
For oral administration.
| ||||||||||||||||||||||||||||||||||||||
| Withdrawal times: | ||||||||||||||||||||||||||||||||||||||
| None. | ||||||||||||||||||||||||||||||||||||||
| Warning: | ||||||||||||||||||||||||||||||||||||||
| Keep out of reach of children. | ||||||||||||||||||||||||||||||||||||||
| Packing: | ||||||||||||||||||||||||||||||||||||||
| Bottle containing 1000 ml., can 5, 10, 200 or 1000 litres. | ||||||||||||||||||||||||||||||||||||||
| Form of product | : Oral liquids |
| Type of product | : Amino Acids |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Amino acids |
| Powder for oral administration | ||||||||||||||||||||||||||||||||||||||
| Composition: | ||||||||||||||||||||||||||||||||||||||
Contains per gram powder:
| ||||||||||||||||||||||||||||||||||||||
| Description: | ||||||||||||||||||||||||||||||||||||||
| Amino acids are essential for the proper operation of numerous physiological functions. They play central roles both as building blocks of proteins and as key intermediates in metabolism.
| ||||||||||||||||||||||||||||||||||||||
| Indications: | ||||||||||||||||||||||||||||||||||||||
| Aminogrow WS is a well balanced combination of essential amino acids for calves, cattle, goats, poultry, sheep and swine. Aminogrow WS is used for:
- Prevention or treatment of amino acids deficiencies in farm animals. - Prevention or treatment of stress, caused for instance by vaccination, diseases, transport, high humidity, high temperatures or extreme temperature changes. - Improvement of feed conversion. | ||||||||||||||||||||||||||||||||||||||
| Side effects: | ||||||||||||||||||||||||||||||||||||||
| No undesirable effects are to be expected when the prescribed dosage regimen is followed. | ||||||||||||||||||||||||||||||||||||||
| Dosage: | ||||||||||||||||||||||||||||||||||||||
For oral administration.
| ||||||||||||||||||||||||||||||||||||||
| Withdrawal times: | ||||||||||||||||||||||||||||||||||||||
| None. | ||||||||||||||||||||||||||||||||||||||
| Warning: | ||||||||||||||||||||||||||||||||||||||
| Keep out of reach of children. | ||||||||||||||||||||||||||||||||||||||
| Packing: | ||||||||||||||||||||||||||||||||||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | ||||||||||||||||||||||||||||||||||||||
| Form of product | : Water soluble powders |
| Type of product | : Amino Acids |
| Suited for animals | : Cattle (cows),Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Amoxycillin trihydrate |
| Oily suspension for parenteral use | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| Description: | ||||||
| Ampicillin is a semi-synthetic broad-spectrum penicillin with bactericidal action against both Gram-positive and Gram-negative bacteria. The range of effect includes Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothirx, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp.
The bacterial action is due to inhibition of cell wall synthesis. Ampicillin is mainly excreted in urine. A major part can also be excreted in bile. | ||||||
| Indications: | ||||||
| Gastrointestinal, respiratory and urogenital infections and mastitis caused by for ampicillin sensitive microorganisma, like E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp., in cattle, calves, swine, sheep and goats. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to ampicillin.
Administration to animals with a serious impaired renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. | ||||||
| Side effects: | ||||||
| Hypersensitivity reactions. | ||||||
| Dosage: | ||||||
For intramuscular or subcutaneous administration:
Shake well before use and do not administer more than 20 ml. in cattle, more than 10 ml. in swine and more than 5 ml. in calves, sheep and goats per injection site. | ||||||
| Withdrawal times: | ||||||
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Vial of 100 ml. | ||||||
| Form of product | : Injectables |
| Type of product | : Antibiotics (Penicillins) |
| Suited for animals | : Cattle (cows),Goats,Sheep,Pigs (swine),Calves |
| Active ingredients | : Ampicillin trihydrate |
| Powder for oral administration | |||||||||||
| Composition: | |||||||||||
Contains per gram powder:
| |||||||||||
| Description: | |||||||||||
| Amprolium is an anticoccidial with activity against Eimeria spp., especially Eimeria tenella
and Eimeria necatrix. Sulfaquinoxaline is a chemotherapeutics with a bacteriostatic activity against many grampositive and gramnegative bacteria and has also coccidiostatic activity against Eimeria spp. | |||||||||||
| Indications: | |||||||||||
| Coccidiosis in calves, sheep, goats and poultry. | |||||||||||
| Contra indications: | |||||||||||
| Administration to animals with impaired liver and/or renal function.
Hypersensitivity to amprolium and/or sulfaquinoxaline. | |||||||||||
| Side effects: | |||||||||||
| At high dosages in laying-hens egg-drop and in broilers growth inhibition and polyneuritis can occur. Crystalluria, anaemie, leucopenia and thrombocytopenia. | |||||||||||
| Dosage: | |||||||||||
For oral administration:
Note: for pre-ruminant calves, lambs and kids only. Do not administer to hens producing eggs for human consumption. | |||||||||||
| Withdrawal times: | |||||||||||
- For meat:
| |||||||||||
| Warning: | |||||||||||
| Keep out of reach of children. | |||||||||||
| Packing: | |||||||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | |||||||||||
| Form of product | : Water soluble powders |
| Type of product | : Coccidiostatics |
| Suited for animals | : Poultry,Sheep,Calves |
| Active ingredients | : Amprolium.HCl,Sulfaquinoxaline sodium,Vitamins |
| Powder for oral administration. | ||||||||||||
| Composition: | ||||||||||||
Contains per gram powder:
| ||||||||||||
| Description: | ||||||||||||
| Amprolium is a coccidiostat (antiprotozoal) used for the treatment and prevention of coccidiosis in calves, goats, sheep, chickens (broilers and breeders) and other fowl such as turkeys, with activity against Eimeria spp., especially Eimeria tenella and Eimeria necatrix. It is a thiamine (vitamin B1) analogue and its pharmacological effect relies on competitive inhibition of thiamine uptake. Amprolium competitively inhibits the active transport of thiamine in isolated second-generation schizonts of Eimeria spp., and in host intestinal cells. Upon ingestion of amprolium, the coccidia experience thiamin deficiency and starve from malnutrition. | ||||||||||||
| Indications: | ||||||||||||
| Amprolin-300 WS is indicated for coccidiosis caused by coccidia susceptible to amprolium (Eimeria spp.), or gastrointestinal infections for which it is therapeutically or prophylactically indicated to administer amprolium, in calves, goats, sheep and poultry. | ||||||||||||
| Contra indications: | ||||||||||||
| The use of amprolium is prohibited from a laying age onwards. Do not administer to poultry whose eggs are intended for human consumption, or to animals with impaired liver and/or renal functions. Do not administer to turkeys before the age of 8 to 10 weeks. | ||||||||||||
| Side effects: | ||||||||||||
| Overdosage of amprolium can suppress weight gain in broilers and cause polyneuritis. Long-term administration of amprolium in high doses may result in thiamine (vitamin B1) deficiency in the host. To treat amprolium overdose, thiamine should be administered parenterally or orally. | ||||||||||||
| Dosage: | ||||||||||||
| For oral administration:
Calves, goats, sheep:
Poultry:
Note: Mix Amprolin-300 WS daily with fresh water. Not intended for hens producing eggs for human consumption. In severe cases curative treatment may be followed by preventive treatment. | ||||||||||||
| Withdrawal times: | ||||||||||||
-For meat:
| ||||||||||||
| Warning: | ||||||||||||
| Keep out of reach of children. | ||||||||||||
| Packing: | ||||||||||||
| Sachet of 100 g and jar of 500 and 1000 g. | ||||||||||||
| Form of product | : Water soluble powders |
| Type of product | : Coccidiostatics |
| Suited for animals | : Goats,Poultry,Sheep,Calves |
| Active ingredients | : Amprolium.HCl |
| Effervescent Disinfectant Tablets | |||||||||||||
| Composition: | |||||||||||||
| |||||||||||||
| Description: | |||||||||||||
| Aquapure are effervescent tablets used primarily for the disinfection of farm water. These tablets are also used for disinfection of surfaces and equipment on farms.
They are soluble tablets which, when dissolved in water, give a measured dose of hypochlorous acid (measurable as free available chlorine) and thereby provide a convenient, economical and accurate method of disinfection on farms. Water treated with Aquapure will be microbially safe for consumption by all farm animals. The active constituent of Aquapure is sodium dichloroisocyanurate (sodium troclosene). On addition to water, it releases hypochlorous acid (measurable as free available chlorine), and monosodium cyanurate (a non-toxic and biodegradable compound) | |||||||||||||
| Indications: | |||||||||||||
| Aquapure Tablets are effective against a broad spectrum of Bacteria (like Actinobacillus pleuropneumonia, Aeromonas hydrophila, Bacillus anthracis, Bacillus intestalis, Bordetella bronchiseptica, Brachispira, Brucella spp., Campylobacter spp., Enterobacter cloacae, Enterococcus faecium, Erysipelotrix rhusopathiae, Escherichia coli, Klebsiella pneumoniae, Leptospira interrogans, Listeria monocytogenes, Mycobacterium spp, Mycoplasme spp., Pasturella multicoda, Plesiomonas shigelloides, Proteus vulgaris, Pseudomonas spp., Salmonella spp., Staphylococcus aureus, Streptococcus spp. and Yersinia spp.), Fungi (Aspergillus spp., Candida albicans and Scopulariopsis brevicaulis), Spores (like Bacillus spp., Clostridium spp.), Viruses (like Adenovirus, Aujeszkey’s disease, Avipox, Rabies, Gumboro disease, Marek’s disease, Avian influenza, Africanswine fever, Foot and mouth disease, Hepatitis, Newcastle disease virus, Avipox virus, Swine Vesicular disease, Porcine parvovirus, Talfan and Reovirus) and Protozoa. | |||||||||||||
| Dosage: | |||||||||||||
Aquapure Tablets are used for the provision of clean, safe drinking water for farm animals.
Dosage (disinfection of surfaces and equipment on farms): Aquapure Tablets are used for disinfection of surfaces and equipment on farms.
| |||||||||||||
| Withdrawal times: | |||||||||||||
| None. | |||||||||||||
| Warning: | |||||||||||||
| Keep out of reach of children. | |||||||||||||
| Packing: | |||||||||||||
| 60 tablets per jar. | |||||||||||||
| Form of product | : Disinfectants |
| Type of product | : Disinfectants |
| Suited for animals | : Camels |
| Active ingredients | : Sodium dichloroisocyanurate |
| Effervescent Desinfectant Tablets | ||||||||||
| Composition: | ||||||||||
| ||||||||||
| Description: | ||||||||||
| Aquapure are effervescent tablets used primarily for the desinfection of farm water. These tablets are also used for desinfection of surfaces and equipment on farms.
They are soluble tablets which, when dissolved in water, give a measured dose of hypochlorous acid (measurable as free available chlorine) and thereby provide a convenient, economical and accurate method of desinfection on farms. Water treated with Aquapure will be microbially safe for consumption by all farm animals. The active constituent of Aquapure is sodium dichloroisocyanurate (sodium troclosene). On addition to water, it releases hypochlorous acid (measurable as free available chlorine), and monosodium cyanurate (a non-toxic and biodegradable compound). | ||||||||||
| Indications: | ||||||||||
| Aquapure Tablets are effective against a broad spectrum of Bacteria (like Actinobacillus pleuropneumonia, Aeromonas hydrophila, Bacillus anthracis, Bacillus intestalis, Bordetella bronchiseptica, Brachispira, Brucella spp., Campylobacter spp., Enterobacter cloacae, Enterococcus faecium, Erysipelotrix rhusopathiae, Escherichia coli, Klebsiella pneumoniae, Leptospira interrogans, Listeria monocytogenes, Mycobacterium spp, Mycoplasme spp., Pasturella multicoda, Plesiomonas shigelloides, Proteus vulgaris, Pseudomonas spp., Salmonella spp., Staphylococcus aureus, Streptococcus spp. and Yersinia spp.), Fungi (Aspergillus spp., Candida albicans and Scopulariopsis brevicaulis), Spores (like Bacillus spp., Clostridium spp.), Viruses (like Adenovirus, Aujeszkey’s disease, Avipox, Rabies, Gumboro disease, Marek’s disease, Avian influenza, Africanswine fever, Foot and mouth disease, Hepatitis, Newcastle disease virus, Avipox virus, Swine Vesicular disease, Porcine parvovirus, Talfan and Reovirus) and Protozoa | ||||||||||
| Contra indications: | ||||||||||
| None. | ||||||||||
| Side effects: | ||||||||||
| None. | ||||||||||
| Dosage: | ||||||||||
| Dosage (desinfection farm water) :
Aquapure Tablets are used for the provision of clean, safe drinking water for farm animals.
Dosage (desinfection of surfaces and equipment on farms): Aquapure tablets are used for desinfection of surfaces and equipment on farms.
| ||||||||||
| Withdrawal times: | ||||||||||
| None. | ||||||||||
| Warning: | ||||||||||
| Keep out of reach of children. | ||||||||||
| Packing: | ||||||||||
| 200 tablets per jar. | ||||||||||
| Form of product | : Disinfectants |
| Type of product | : Disinfectants |
| Suited for animals | : Camels |
| Active ingredients | : Sodium dichloroisocyanurate |
| Aqueous solution for parenteral use | |||||||||
| Composition: | |||||||||
| |||||||||
| Description: | |||||||||
| Flunixin is a non-steroidal anti-inflammatory drug (NSAID), and a non-narcotic analgesic with antipyretic properties. It is used in the allevation of inflammation and pain associated with musculo-skeletal disorders and colic. In addition it is used for the control of acute inflammation reactions associated with infectious diseases. Flunixin is also applied as adjunctive therapy in the treament of respiratory diseases. | |||||||||
| Indications: | |||||||||
| Cattle: Banixin-50 is indicated as an adjunct to antimicrobial therapy to reduce clinical signs of acute inflammation in cases of infectious respiratory disease.
Horses: Banixin-50 is indicated for the alleviation of inflammatory signs associated with musculo-skeletal disorders and for the alleviation of visceral pain associated with colic. Swine: Banixin-50 is indicated as an adjunctive therapy in the treatment of swine respiratory diseases. | |||||||||
| Contra indications: | |||||||||
| Do not exceed the recommended dose or duration of treatment.
Do not administer to pregnant mares or sows, or to dehydrated, hypovolaemic or hypotensive animals. Do not use in lactating mares producing milk for human consumption. Banixin-50 is contraindicated in animals suffering from cardiac, hepatic or renal disease, where there is the possibility of gastro-intestinal ulceration or bleeding, where there is evidence of a blood dyscrasia or hypersensitivity to the product. Do not administer to animals undergoing general anaesthesia until fully recovered. Avoid intra-arterial injection or concurrent administration of other NSAIDs and nephrotoxic drugs. Use in any animal less than 6 weeks of age or in aged animals may involve additional risks. | |||||||||
| Side effects: | |||||||||
| Adverse reactions include gastro-intestinal irritation, ulceration, changes in haematology and - in dehydrated, hypovolaemic or hypotensive animals - a potential for renal damage.
In rare cases, severe analphylactoid reactions have been observed, ocassionally with fatal outcome. | |||||||||
| Dosage: | |||||||||
For intramuscular or intravenous administration:
Inject the product slowly, and apply at body temperature. Administration should be stopped immediately if signs of intolerance occur. An adequate water supply should be provided. | |||||||||
| Withdrawal times: | |||||||||
| - For meat:
Cattle: 14 days. Horses: 28 days. Pigs: 24 days. - For milk: Cattle: 2 days. | |||||||||
| Warning: | |||||||||
| Keep out of reach of children. | |||||||||
| Packing: | |||||||||
| Vial of 50 ml. | |||||||||
| Form of product | : Injectables |
| Type of product | : Analgesics,Anti-inflammatories |
| Suited for animals | : Cattle (cows),Horses,Pigs (swine) |
| Active ingredients | : Flunixin meglumine |
| oily suspension for parenteral use | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| Description: | ||||||
| Amoxycillin is a semisynthetic broad-spectrum penicillin with a bactericidal action against both Gram-positive and Gram-negative bacteria. The range of effect includes Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp. The bactericidal action is due to inhibition of cell wall synthesis. Amoxycillin is mainly excreted in urine. A major part can also be excreted in bile. | ||||||
| Indications: | ||||||
| Gastrointestinal, respiratory and urinary tract infections caused by amoxycillin sensitive micro-organisms, like Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp., in calves, cattle, goats, sheep and swine. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to amoxycillin.
Administration to animals with a serious impaired renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. | ||||||
| Side effects: | ||||||
| Hypersensitivity reactions. | ||||||
| Dosage: | ||||||
For intramuscular or subcutaneous administration:
Shake well before use and do not administer more than 20 ml. in cattle, more than 10 ml. in swine and more than 5 ml. in calves, sheep and goats per injection site. | ||||||
| Withdrawal times: | ||||||
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Vial of 100 ml. | ||||||
| Form of product | : Injectables |
| Type of product | : Antibiotics (Penicillins) |
| Suited for animals | : Cattle (cows),Goats,Sheep,Pigs (swine),Calves |
| Active ingredients | : Amoxycillin trihydrate |
| Oily suspension for parenteral use | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| Description: | ||||||
| Amoxycillin is a semisynthetic broad-spectrum penicillin with a bactericidal action against both Gram-positive and Gram-negative bacteria. The range of effect includes Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp. The bactericidal action is due to inhibition of cell wall synthesis. Amoxycillin is mainly excreted in urine. A major part can also be excreted in bile. | ||||||
| Indications: | ||||||
| Gastrointestinal, respiratory and urinary tract infections caused by amoxycillin sensitive micro-organisms, like Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp., in calves, cattle, goats, sheep and swine. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to amoxycillin.
Administration to animals with a serious impaired renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. | ||||||
| Side effects: | ||||||
| Hypersensitivity reactions. | ||||||
| Dosage: | ||||||
| For intramuscular or subcutaneous administration:
General: 1 ml. per 10 kg. body weight, repeatable if necessary after 48 hours. Shake well before use and do not administer more than 20 ml. in cattle, more than 10 ml. in swine and more than 5 ml. in calves, sheep and goats per injection site. | ||||||
| Withdrawal times: | ||||||
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Vial of 100 ml. | ||||||
| Form of product | : Injectables |
| Type of product | : Antibiotics (Penicillins) |
| Suited for animals | : Cattle (cows),Goats,Sheep,Pigs (swine),Calves |
| Active ingredients | : Amoxycillin trihydrate |
| Powder for oral administration | ||||||
| Composition: | ||||||
Contains per gram powder:
| ||||||
| Description: | ||||||
| Amoxycillin is a semisynthetic broad-spectrum penicillin with a bactericidal action against both Gram-positive and Gram-negative bacteria. The range of effect includes Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp. The bactericidal action is due to inhibition of cell wall synthesis. Amoxycillin is mainly excreted in urine. A major part can also be excreted in bile. | ||||||
| Indications: | ||||||
| Gastrointestinal, respiratory and urinary tract infections caused by amoxycillin sensitive micro-organisms, like Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, penicillinase negative Staphylococcus and Streptococcus spp., in calves, goats, poultry, sheep and swine. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to amoxycillin.
Administration to animals with a serious impaired renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. Administration to animals with an active microbiological digestion. | ||||||
| Side effects: | ||||||
| Hypersensitivity reaction. | ||||||
| Dosage: | ||||||
For oral administration:
Note: for pre-ruminant calves, lambs and kids only. | ||||||
| Withdrawal times: | ||||||
- For meat:
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | ||||||
| Form of product | : Water soluble powders |
| Type of product | : Antibiotics (Penicillins) |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Amoxycillin trihydrate |
| Composition: | |||||||||||||
Contains per ml:
| |||||||||||||
| Description: | |||||||||||||
| The combination of amoxicillin and gentamicin acts synergistically against a wide range of infections caused by both Gram-positive (e.g. Staphylococcus, Streptococcus and Corynebacterium spp.) and Gram-negative (e.g. E.coli, Pasteurella, Salmonella and Pseudomonas spp.) bacteria in cattle and swine. Amoxicillin inhibits mainly in Gram-positive bacteria the cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell wall. Gentamicin binds to the 30S subunit of the ribosome of mainly Gram-negative bacteria, thereby interrupting protein synthesis. Excretion of Biogenta occurs mainly unchanged via urine, and to a lesser degree via milk. | |||||||||||||
| Indications: | |||||||||||||
| Cattle: gastrointestinal, respiratory and intramammary infections caused by bacteria sensitive to the combination of amoxicillin and gentamicin, such as pneumonia, diarrhoea, bacterial enteritis, mastitis, metritis and cutaneous abscesses.
Swine: respiratory and gastrointestinal infections caused by bacteria sensitive to the combination of amoxicillin and gentamicin, such as pneumonia, colibacillosis, diarrhoea, bacterial enteritis and mastitis-metritis-agalactia syndrome (MMA). | |||||||||||||
| Contra indications: | |||||||||||||
| Hypersensitivity towards amoxicillin or gentamicin.
Administration to animals with a seriously impaired liver and/or renal function. Concurrent administration of tetracyclines, chloramphenicol, macrolides and lincosamides. Concurrent administration of nephrotoxic compounds | |||||||||||||
| Side effects: | |||||||||||||
| Hypersensitivity reactions. | |||||||||||||
| Dosage: | |||||||||||||
For intramuscular administration. The general dosage is 1 ml per 10 kg body weight per day for 3 days.
| |||||||||||||
| Withdrawal times: | |||||||||||||
| |||||||||||||
| Warning: | |||||||||||||
| Keep out of reach of children. | |||||||||||||
| Packing: | |||||||||||||
| Vial of 100 ml. | |||||||||||||
| Form of product | : Injectables |
| Type of product | : Penicillins,Antibiotics (Non penicillins),Antibiotics (Penicillins) |
| Suited for animals | : Cattle (cows),Pigs (swine),Calves,Piglets |
| Active ingredients | : Amoxycillin trihydrate,Gentamycin sulphate |
| Suspension for intramammary administration | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| Description: | ||||||
| The combination of amoxycillin and neomycin acts additive. Amoxycillin is a semisynthetic broad-spectrum penicillin with a bactericidal action against both Gram-positive and Gram-negative bacteria. The range of effect includes Campylobacter, Clostridium, Corynebacterium, E. coli, Erysipelothrix, Haemophilus, Pasteurella, Salmonella, Streptococcus spp. and penicillinase negative Staphylococcus. The bactericidal action is due to inhibition of cell wall synthesis. Neomycin is an aminoglycoside with a bactericidal action against mainly Gram-negative bacteria like E. coli, Klebsiella, Pasteurella, Salmonella and Staphylococcus spp. | ||||||
| Indications: | ||||||
| Treatment of clinical mastitis caused by amoxycillin and neomycin sensitive micro-organisms like, Corynebacterium, E. coli, Staphylococcus and Streptococcus spp. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to amoxycillin and/or neomycin.
Administration in subtherapeutic doses. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. Administration to animals with a serious impaired renal and/or liver function. Overdosages because of the small safety margin of neomycin. | ||||||
| Side effects: | ||||||
| Hypersensitivity reactions.
Renal dysfunction, neurotoxicity and neuromuscular blockade. | ||||||
| Dosage: | ||||||
| For intramammary administration:
Daily 1 injector per affected quarter for maximal 3 days. Before application quarters have to be fully stripped and teats have to be cleaned and disinfected. | ||||||
| Withdrawal times: | ||||||
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Injector of 5 ml. | ||||||
| Form of product | : Miscellaneous |
| Type of product | : Antibiotics (Penicillins),Intramammaries |
| Suited for animals | : Cattle (cows) |
| Active ingredients | : Amoxycillin trihydrate,Neomycin sulphate |
| solution for parenteral use | ||||||
| Composition: | ||||||
Contains per ml.:
| ||||||
| 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: | ||||||
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Glass vial of 50 ml. | ||||||
| Form of product | : Injectables |
| Type of product | : Theileriosis |
| Suited for animals | : Cattle (cows) |
| Active ingredients | : Buparvaquone |
| Aqueous solution for parenteral use. | ||||||||||||||||||||||||
| Composition: | ||||||||||||||||||||||||
Contains per ml.:
| ||||||||||||||||||||||||
| Description: | ||||||||||||||||||||||||
| Butafosfan is an organic phosphorus compound used as an injectable source of phosphorus in animals that takes part in energy metabolism, replenishes serum phosphorus levels, supports liver function and stimulates fatigued smooth and cardiac muscle. Its physiological rather than its pharmacological action accounts for its very low level of toxicity. Cyanocobalamin (vitamin B12) assist in various metabolic processes, most notably the formation of red blood cells, and stimulates protein, carbohydrate and fat metabolism. | ||||||||||||||||||||||||
| Indications: | ||||||||||||||||||||||||
| Butasal-100 is indicated for debilitation by acute or chronic metabolism disorders that result from poor nutrition, inadequate management or disease (e.g. developmental and nutritional disorders in young animals due to rearing disease, and (secondary) ketosis in cows). It can be used for metaphylaxis of infertility, puerperal diseases and in support of sterility treatment. It acts as a roborant in cases of stress, overexertion, exhaustion and reduced resistance, and as a tonic in cases of weakness, secondary anaemia and chilling. Butasal-100 additionally supports muscular physiology, the treatment of infertility, and tetany and paresis as an adjunct to calcium and magnesium therapy. | ||||||||||||||||||||||||
| Contra indications: | ||||||||||||||||||||||||
| No contra-indications have been identified for Butasal-100 or any of its constituents. | ||||||||||||||||||||||||
| Side effects: | ||||||||||||||||||||||||
| No undesirable effects are known for this product. | ||||||||||||||||||||||||
| Dosage: | ||||||||||||||||||||||||
For intravenous, intramuscular or subcutaneous administration:
- Repeat daily if required. - In cases of chronic disease: half the dose at intervals of 1 - 2 weeks or less. - In healthy animals: half the dose. | ||||||||||||||||||||||||
| Withdrawal times: | ||||||||||||||||||||||||
| ||||||||||||||||||||||||
| Warning: | ||||||||||||||||||||||||
| Keep out of reach of children. | ||||||||||||||||||||||||
| Packing: | ||||||||||||||||||||||||
| Glass vial of 100 ml. | ||||||||||||||||||||||||
| Form of product | : Injectables |
| Type of product | : Growth stimulators,Vitamins |
| Suited for animals | : Cats,Cattle (cows),Dogs,Goats,Horses,Poultry,Sheep,Pigs (swine),Calves,Lambs,Kids,Piglets |
| Active ingredients | : Butafosfan,Vitamins |
| Powder for oral administration | ||||||
| Composition: | ||||||
Contains per gram powder:
| ||||||
| Description: | ||||||
| Chlortetracycline belongs to the group of tetracyclines and acts bacteriostatic against many Gram-positive and Gram-negative bacteria like Bordetella, Campylobacter, Chlamydia, E. coli, Haemophilus, Mycoplasma, Pasteurella, Rickettsia, Salmonella, Staphylococcus and Streptococcus spp. The action of chlortetracycline is based on inhibition of bacterial protein synthesis. Chlortetracycline is mainly excreted in urine, for a small part in bile and in lactating animals in milk. | ||||||
| Indications: | ||||||
| Gastrointestinal and respiratory infections caused by Chlortetracycline sensitive bacteria, like Bordetella, Campylobacter, Chlamydia, E. coli, Haemophilus, Mycoplasma, Pasteurella, Rickettsia, Salmonella, Staphylococcus and Streptococcus spp., in calves, goats, poultry, sheep and swine. | ||||||
| Contra indications: | ||||||
| Hypersensitivity to tetracyclines.
Administration to animals with a serious impaired renal and/or liver function. Concurrent administration with bactericidal agents like penicillins. Administration to animals with an active microbiological digestion. | ||||||
| Side effects: | ||||||
| Discoloration of teeth in young animals.
Hypersensitivity reactions. | ||||||
| Dosage: | ||||||
For oral administration through drinking-water.
Note: for pre-ruminant calves, lambs and kids only. | ||||||
| Withdrawal times: | ||||||
- for meat
| ||||||
| Warning: | ||||||
| Keep out of reach of children. | ||||||
| Packing: | ||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | ||||||
| Form of product | : Water soluble powders |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Chlortetracycline.HCl |
| Aqueous solution for parenteral use. | ||||||||||||||
| Composition: | ||||||||||||||
Contains per ml.:
| ||||||||||||||
| Description: | ||||||||||||||
| Acepromazine is a neuroleptic belonging to the phenothiazines with a sedative action. The effect is set in within 5 10 minutes after intravenous injection and within 15-20 minutes after intramuscular injection and is maintained for 6 to 12 hours. | ||||||||||||||
| Indications: | ||||||||||||||
| All situations where sedation is needed, for instance during transport, with several forms of stress, small operations and as a pre anaesthetic with larger operations. | ||||||||||||||
| Contra indications: | ||||||||||||||
| Administration to animals with heart or respiratory diseases.
Administration together with local anaesthetics (like procaine) or organo-phosphates (like insecticides) because acepromazine potentates toxicity of these compounds. Hypothermia or hypertension. | ||||||||||||||
| Side effects: | ||||||||||||||
| After high doses respiratory disorders, hypertensy and tachydardy can occur.
Penis relaxation in male animals. | ||||||||||||||
| Dosage: | ||||||||||||||
| For intramuscular or intravenous administration.
Calves, cattle, horses and swine:
| ||||||||||||||
| Withdrawal times: | ||||||||||||||
| ||||||||||||||
| Warning: | ||||||||||||||
| Keep out of reach of children. | ||||||||||||||
| Packing: | ||||||||||||||
| Vial of 100 ml. | ||||||||||||||
| Form of product | : Injectables |
| Type of product | : Sedatives |
| Suited for animals | : Cats,Cattle (cows),Dogs,Horses,Pigs (swine),Calves |
| Active ingredients | : Acepromazine maleate |
| Oily suspension for parenteral use. | ||||||||||||||
| Composition: | ||||||||||||||
| ||||||||||||||
| Description: | ||||||||||||||
| Ceftiofur is a semisynthetic, third generation, broad-spectrum cephalosporin antibiotic, which is administered to cattle and swine for control of bacterial infections of the respiratory tract, with additional action against foot rot and acute metritis in cattle. It has a wide spectrum of activity against both Gram-positive and Gram-negative bacteria. It exerts its antibacterial action by inhibition of cell wall synthesis. Ceftiofur is mainly excreted in urine and faeces. | ||||||||||||||
| Indications: | ||||||||||||||
| Cattle: Ceftionel-50 oily suspension is indicated for treatment of the following bacterial diseases: Bovine respiratory disease (BRD, shipping fever, pneumoniae) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni (Haemophilus somnus); acute bovine interdigital necrobacillosis (foot rot, pododermatitis) associated with Fusobacterium necrophorum and Bacteroides melaninogenicus; Acute metritis (0 to 10 days post-partum) associated with bacterial organisms such as E.coli, Arcanobacterium pyogenes and Fusobacterium necrophorum.
Swine: Ceftionel-50 oily suspension is indicated for treatment/control of swine bacterial respiratory disease (swine bacterial pneumoniae) associated with Actinobacillus (Haemophilus) pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis and Streptococcus suis. | ||||||||||||||
| Contra indications: | ||||||||||||||
| Hypersensitivity to cephalosporins and other β-lactam antibiotics.
Administration to animals with a serious impaired renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. | ||||||||||||||
| Side effects: | ||||||||||||||
| Mild hypersensitivity reactions may occur occasionally at the injection site, which subside without further treatment. | ||||||||||||||
| Dosage: | ||||||||||||||
Cattle:
Shake well before use and do not administer more than 15 ml in cattle per injection site and not more than 10 ml in swine. Successive injections should be administered at different sites. | ||||||||||||||
| Withdrawal times: | ||||||||||||||
| ||||||||||||||
| Warning: | ||||||||||||||
| Keep out of reach of children. | ||||||||||||||
| Packing: | ||||||||||||||
| Vial of 100 ml. | ||||||||||||||
| Form of product | : Injectables |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Cattle (cows),Pigs (swine) |
| Active ingredients | : Ceftiofur sodium |
| Solution for oral administation. | |||||||||||
| Composition: | |||||||||||
| |||||||||||
| Description: | |||||||||||
| Ciprofloxacin belongs to the group of quinolones and acts bactericidal against mainly Gram negative bacteria like Campylobacter, E. coli, Haemophilus, Mycoplasma, Pasteurella and Salmonella spp. | |||||||||||
| Indications: | |||||||||||
| Gastrointestinal, respiratory and urinary tract infections caused by Ciprofloxacin sensitive micro-organisms, like Campylobacter, E. coli, Haemophilus, Mycoplasma, Pasteurella and Salmonella spp., in calves, goats, poultry, sheep and swine. | |||||||||||
| Contra indications: | |||||||||||
| Hypersensitivity to ciprofloxacin.
Administration to animals with a serious impaired liver and/or renal function. Concurrent administration with tetracyclines, chloramphenicol, macrolides and lincosamides. | |||||||||||
| Side effects: | |||||||||||
| Hypersensitivity reactions.
Administration to juvenile animals can lead to arthropathy. | |||||||||||
| Dosage: | |||||||||||
For oral administration:
Note: for pre-ruminant calves, lambs and kids only. | |||||||||||
| Withdrawal times: | |||||||||||
| - For meat: 12 days. | |||||||||||
| Warning: | |||||||||||
| Keep out of reach of children. | |||||||||||
| Packing: | |||||||||||
| Bottle containing 100, 500 and 1000 ml. | |||||||||||
| Form of product | : Oral liquids |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Ciprofloxacin |
| Injectable solution for parenteral use | ||||
| Composition: | ||||
Contains per ml.:
| ||||
| Description: | ||||
|
Cloprostenol is a synthetic prostaglandin analogue structurally related to Prostaglandin F2µ (PGF2µ), for use in cattle and horses. As a potent luteolytic agency it causes functional and morphological regression of the corpus luteum (luteolysis) in cattle and horses followed by return to oestrus and normal ovulation. | ||||
| Indications: | ||||
| Cattle: - Functional ovarian disorders such as anoestrus due to persistent corpus luteum, suboestrus, luteal or follicular cysts. - Synchronisation of oestrus. - Induction of parturition or abortion (associated increased incidence of retained foetal membranes, retentio secundinarum). Postpuerperium disorders of the uterus (e.g. pyometra, endometritis). Mares: - Induction of oestrus in cycling mares (at day 5-13 of cycle). - Induction of abortion during the first 35 days of pregnancy. | ||||
| Contra indications: | ||||
| Do not administer to pregnant animals, unless the objective is to terminate pregnancy. Do not administer to horses intended for human consumption. | ||||
| Side effects: | ||||
| Use for induction of parturition or abortion in cattle is accompanied by an increased incidence of retained foetal membranes. | ||||
| Dosage: | ||||
| For intramuscular administration: Cattle: 2 ml. per single or repeated dose. Mares: 1 - 2 ml. per single dose. Ponies and donkies: 0.5 - 1 ml. per single dose. | ||||
| Withdrawal times: | ||||
| - For meat : 1 days. - For milk : 0 days. | ||||
| Warning: | ||||
| Packing: | ||||
| Vial of 10 ml. | ||||
| Form of product | : Injectables |
| Type of product | : Hormones |
| Suited for animals | : Cattle (cows),Horses |
| Active ingredients | : Cloprostenol sodium |
| Aqueous solution for parenteral use. | |||||
| Composition: | |||||
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| Description: | |||||
| Closantel is active against fasciola and hypoderma spp. | |||||
| Indications: | |||||
| Prophylaxis and treatment of worminfections in calves, cattle, goats, sheep
like: Fasciola, Hypoderma, Oestrus spp. | |||||
| Contra indications: | |||||
| Administration to lactating animals. | |||||
| Side effects: | |||||
| Overdoses can cause colic, coughing, excessive salivation, excitation, hyperpnoea, lachrymation, spasms, sweating and vomiting. | |||||
| Dosage: | |||||
For subcutaneous administration:
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| Withdrawal times: | |||||
| - For meat: 28 days. | |||||
| Warning: | |||||
| Keep out of reach of children. | |||||
| Packing: | |||||
| Vial of 100 and 250 ml. | |||||
| Form of product | : Injectables |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Closantel |
| Aqueous suspension for parenteral use. | |||||||
| Composition: | |||||||
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| Description: | |||||||
| Levamisole is a synthetic anthelmintic with activity against a broad spectrum of gastrointestinal worms and against lung worms. Levamisole causes an increase of the axial muscle tone followed by paralysis of worms. Closanthel is active against fasciola and hypoderma spp. | |||||||
| Indications: | |||||||
| Prophylaxis and treatment of gastrointestinal and lung worminfections like:
Calves, cattle, goats, sheep: Bunostomum, Chabertia, Cooperia, Dictyocaulus, Haemonchus, Hypoderma, Fasciola, Nematodirus, Ostertagia, Protostrongylus and Trichostrongylus spp. Swine : Ascaris suum, Hyostrongylus rubidus, Metastrongylus elongatus, Oesophagostomum spp. and Trichuris suis. | |||||||
| Contra indications: | |||||||
| Administration to animals with an impaired liver function.
Concurrent administration with pyrantel, morantel or organo-phosphates. Do not use to pregnant female aniumals in the last 3th of pregnancy. | |||||||
| Side effects: | |||||||
| Overdoses can cause colic, coughing, excessive salivation, excitation, hyperpnoea, lachrymation, spasms, sweating and vomiting. | |||||||
| Dosage: | |||||||
For subcutaneous administration:
Shake well before use and do not administer more than 20 ml. in cattle, more than 10 ml. in swine and more than 5 ml. in calves, sheep and goats per injection site. | |||||||
| Withdrawal times: | |||||||
| - For meat: 28 days. | |||||||
| Warning: | |||||||
| Keep out of reach of children. | |||||||
| Packing: | |||||||
| Vial of 100 and 250 ml. | |||||||
| Form of product | : Injectables |
| Type of product | : Anthelmintics |
| Suited for animals | : Cattle (cows),Goats,Sheep,Calves |
| Active ingredients | : Closantel,Levamisole.HCl |
| Solution for oral administation. | |||||||||||
| Composition: | |||||||||||
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| Description: | |||||||||||
| The combination of colistin and trimethoprim acts additive. Colistin is an antibiotic from the group of polymyxins with a bactericidal action against Gram-negative bacteria like E. coli, Haemophilus and Salmonella spp. Since colistin is absorbed for a very small part after oral administration only gastrointestinal indications are relevant. Trimethoprim is an antibacterial agent with a bacteriostatic action against many Gram-negative and Gram-positive bacteria like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp. After oral administration trimethoprim is absorbed almost totally and penetrates well into tissues and cells. | |||||||||||
| Indications: | |||||||||||
| Gastrointestinal infections caused by colistin and trimethoprim sensitive micro-organisms, like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp., in kids, lambs and piglets. | |||||||||||
| Contra indications: | |||||||||||
| Hypersensitivity to colistin and/or trimethoprim.
Administration to animals with a serious impaired renal function. | |||||||||||
| Side effects: | |||||||||||
| Renal dysfunction, neurotoxicity and neuromuscular blockade. | |||||||||||
| Dosage: | |||||||||||
For oral administration:
Each pressure on the dosing pump delivers one dose, i.e. 1 ml. | |||||||||||
| Withdrawal times: | |||||||||||
| - For meat : 7 days. | |||||||||||
| Warning: | |||||||||||
| Keep out of reach of children. | |||||||||||
| Packing: | |||||||||||
| Vial of 100 ml. with dosing pump. | |||||||||||
| Form of product | : Oral liquids |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Lambs,Kids,Piglets |
| Active ingredients | : Colistin sulphate,Trimethoprim |
| Powder for oral administration | ||||||||
| Composition: | ||||||||
| ||||||||
| Description: | ||||||||
| The combination of colistin and trimethoprim acts additive. Colistin is an antibiotic from the group of polymyxins with a bactericidal action against Gram-negative bacteria like E. coli, Haemophilus and Salmonella. Since colistin is absorbed for a very small part after oral administration only gastrointestinal indications are relevant. Trimethoprim is an antibacterial agent with a bacteriostatic action against many Gram-negative and Gram-positive bacteria like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp. After oral administration trimethoprim is absorbed almost totally and penetrates well into tissues and cells. | ||||||||
| Indications: | ||||||||
| Gastrointestinal infections caused by colistin and trimethoprim sensitive micro-organisms, like E. coli, Haemophilus, Pasteurella, Salmonella, Staphylococcus and Streptococcus spp., in calves, goats, poultry, sheep and swine. | ||||||||
| Contra indications: | ||||||||
| Hypersensitivity to trimethoprim and/or colistin.
Administration to animals with a serious impaired renal function. Administration to animals with an active microbiological digestion. | ||||||||
| Side effects: | ||||||||
| Renal dysfunction, neurotoxicity and neuromuscular blockade.
| ||||||||
| Dosage: | ||||||||
For oral administration:
Note: for pre-ruminant calves, lambs and kids only. Please note: Before adding to the drinking water make a presolution of 1 kg. Colexin WS per 40 litres water with a temperature of 40 degrees Celsius. | ||||||||
| Withdrawal times: | ||||||||
| - For meat: 7 days. | ||||||||
| Warning: | ||||||||
| Keep out of reach of children. | ||||||||
| Packing: | ||||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | ||||||||
| Form of product | : Water soluble powders |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Colistin sulphate,Trimethoprim |
| Powder for oral administration | |||||||
| Composition: | |||||||
| |||||||
| Description: | |||||||
| Colistin is an antibiotic from the group of polymyxins with a bactericidal action against Gram-negative bacteria like E. coli, Haemophilus and Salmonella. Since colistin is absorbed for a very small part after oral administration only gastrointestinal indications are relevant. | |||||||
| Indications: | |||||||
| Gastrointestinal infections caused by colistin sensitive bacteria, like E. coli, Haemophilus and Salmonella spp., in calves, goats, poultry, sheep and swine. | |||||||
| Contra indications: | |||||||
| Hypersensitivity to colistin.
Administration to animals with a serious impaired renal function. Administration to aminals with an active microbiological digestion. | |||||||
| Side effects: | |||||||
| Renal dysfunction, neurotoxicity and neuromuscular blockade. | |||||||
| Dosage: | |||||||
For oral administration:
Note: for pre-ruminant calves, lambs and kids only. | |||||||
| Withdrawal times: | |||||||
| - For meat : 7 days. | |||||||
| Warning: | |||||||
| Keep out of reach of children. | |||||||
| Packing: | |||||||
| Sachet of 100 gram and jar of 500 & 1000 gram. | |||||||
| Form of product | : Water soluble powders |
| Type of product | : Antibiotics (Non penicillins) |
| Suited for animals | : Goats,Poultry,Sheep,Pigs (swine),Calves |
| Active ingredients | : Colistin sulphate |
| Powder for oral administration | |||||
| Composition: | |||||
| |||||
| Description: | |||||
| Colistin is an antibiotic from the group of polymyxins with a bactericidal action against Gram-negative bacteria like E. coli, Haemophilus and Salmonella. Since colistin is absorbed for a very small part after oral administration only gastrointestinal indications are relevant. | |||||
| Indications: | |||||
| Gastrointestinal infections caused by colistin sensitive bacteria, like E. coli, Haemophilus and Salmonella spp., in calves, goats, poultry, sheep and swine.
| |||||
| Contra indications: | |||||
| Hyperse |