- Cattle, sheep, pigs, dogs, cats
- Antibacterial agent
- Injectable suspension
- 150 mg of amoxicillin trihydrate per 1 ml of the drug
- 50 ml
Antibacterial agent of prolonged action.
One dose delivery.
It is easily absorbed from the injection site and penetrates into most organs and tissues of the animal.
The highest concentration of the antibiotic in blood is noted after 1 - 2 hours and is maintained at therapeutic level for at least 48 hours after parenteral administration of the drug.
Composition: Amoxicillin 15% LA contains amoxicillin trihydrate as an active ingredient, 150 mg in 1 ml, as well as excipients: colloidal silica, sorbitan monooleate, and medium chain triglycerides.
Description: Suspension of white to light yellow color. The suspension may separate into layers during storage, but should become homogenous after vial shaking. In the presence of water, a gelled sludge forms in the suspension.
Purpose: Amoxicillin 15% LA is prescribed for therapeutic purposes in cattle, sheep, pigs, dogs and cats for infectious diseases of the gastrointestinal tract, respiratory tract, urogenital system, joints, soft tissues and skin, necrobacillosis, umbilical infections, atrophic rhinitis, mastitis, metritis and agalactia syndrome, and other bacterial infections whose causative agents are sensitive to amoxicillin.
Contraindications: The animal's hypersensitivity to components of the drug and penicillin group antibiotics, as well as severe liver and/or kidney function disorders. Do not use the drug in any newborn animals, rabbits and guinea pigs.
Dosage and how to use: Amoxycillin 15% LA is administered to animals subcutaneously or intramuscularly once at a dose of 1 ml per 10 kg of animal weight (15 mg of active substance per 1 kg of animal weight). If re-injection of the drug is necessary, the 48-hour interval should not be exceeded, as this may lead to a decrease in therapeutic efficacy.
The maximum volume of the drug for administration in one place should not exceed 20 ml in cattle, 5 ml in pigs, sheep, calves, 2.5 ml in dogs, 1 ml in cats.
Withholding period: Slaughter of animals for meat is allowed not earlier than 28 days after the last administration of Amoxycillin 15% LA. Meat of animals slaughtered before the specified period may be used as feed for fur-bearing animals.
Milk may not be used for human consumption during drug administration and within 96 hours after the last injection. Milk obtained before the expiry of the milk withholding period can be boiled and fed to animals.
Storage life of Amoxycillin 15% LA in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.
- Cattle, sheep, pigs, dogs, cats
- Antibacterial agent
- Injectable suspension
- 150 mg of amoxicillin trihydrate per 1 ml of the drug
- 100 ml
Antibacterial agent of prolonged action.
One dose delivery.
It is easily absorbed from the injection site and penetrates into most organs and tissues of the animal.
The highest concentration of the antibiotic in blood is noted after 1 - 2 hours and is maintained at therapeutic level for at least 48 hours after parenteral administration of the drug.
Composition: Amoxicillin 15% LA contains amoxicillin trihydrate as an active ingredient, 150 mg in 1 ml, as well as excipients: colloidal silica, sorbitan monooleate, and medium chain triglycerides.
Description: Suspension of white to light yellow color. The suspension may separate into layers during storage, but should become homogenous after vial shaking. In the presence of water, a gelled sludge forms in the suspension.
Purpose: Amoxicillin 15% LA is prescribed for therapeutic purposes in cattle, sheep, pigs, dogs and cats for infectious diseases of the gastrointestinal tract, respiratory tract, urogenital system, joints, soft tissues and skin, necrobacillosis, umbilical infections, atrophic rhinitis, mastitis, metritis and agalactia syndrome, and other bacterial infections whose causative agents are sensitive to amoxicillin.
Contraindications: The animal's hypersensitivity to components of the drug and penicillin group antibiotics, as well as severe liver and/or kidney function disorders. Do not use the drug in any newborn animals, rabbits and guinea pigs.
Dosage and how to use: Amoxycillin 15% LA is administered to animals subcutaneously or intramuscularly once at a dose of 1 ml per 10 kg of animal weight (15 mg of active substance per 1 kg of animal weight). If re-injection of the drug is necessary, the 48-hour interval should not be exceeded, as this may lead to a decrease in therapeutic efficacy.
The maximum volume of the drug for administration in one place should not exceed 20 ml in cattle, 5 ml in pigs, sheep, calves, 2.5 ml in dogs, 1 ml in cats.
Withholding period: Slaughter of animals for meat is allowed not earlier than 28 days after the last administration of Amoxycillin 15% LA. Meat of animals slaughtered before the specified period may be used as feed for fur-bearing animals.
Milk may not be used for human consumption during drug administration and within 96 hours after the last injection. Milk obtained before the expiry of the milk withholding period can be boiled and fed to animals.
Storage life of Amoxycillin 15% LA in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.
- Horses, cattle, pigs, sheep, goats, dogs
- Nonsteroidal anti-inflammatory drug
- Injectable solution
- 500 mg of sodium metamizole monohydrate per 1 ml of the drug
- 2 ml
Nonsteroidal anti-inflammatory drug.
Fast pain relief.
Easily absorbed from the injection site.
High concentrations in blood plasma are reached quickly.
Composition: Mirazmizol contains sodium metamizole monohydrate as an active ingredient, 500 mg in 1 ml, as well as water for injection.
Description: Transparent liquid from colorless to light yellow color.
Purpose: Miramisole is used in horses, cattle, sheep, pigs, goats, dogs and cats for neuralgias, febrile conditions, muscular and joint rheumatism, acute and chronic arthritis, acute gastric diseases (e.g., intestinal spasms, flatulence, catarrhal spasm, acute intestinal dilation), endometritis, mastitis, tendovaginitis, mastitis, metritis and agalactia syndrome in pigs.
Contraindications: Hypersensitivity to the active substance of the drug, suppression of hematopoiesis (cytostatic or infectious neutropenia, agranulocytosis), renal failure, liver failure, hereditary hemolytic anemia.
Dosage and how to use:
Miramisol is used 2 - 3 times a day for 3 to 5 days in the following dosage:
For cattle, sheep, or goats: intravenous or intramuscular administration of 20 - 40 mg/kg of body weight (0.04 - 0.08 ml/kg) every 8 - 12 hours.
Pigs: intramuscular administration of 15 to 50 mg/kg body weight (0.03 to 0.1 ml/kg) every 8 to 12 hours.
Horses: intravenous or intramuscular administration of 20 - 50 mg/kg of body weight (0.04 - 0.1 ml/kg) every 8 - 12 hours.
Dogs and cats: intravenous, intramuscular or subcutaneous administration of 20 - 25 mg per kg body weight (0.04 - 0.05 ml/kg) every 8 - 12 hours.
Withholding period: Slaughter of animals for meat is allowed not earlier than 12 days after the last administration of Metamizole. If slaughter is necessary before the specified time, the meat may be used to feed carnivorous animals.
Milk of cows, goats and sheep can be used for human consumption 4 days after the last administration of Metamizole. Milk obtained during treatment of animals with the drug and before the expiry of the specified period may be used to feed carnivorous animals.
Storage life of Miramisol in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.
- Cattle, sheep, pigs, dogs, cats
- Antibacterial agent
- Injectable suspension
- 150 mg of amoxicillin trihydrate per 1 ml of the drug
- 100 ml
Antibacterial agent of prolonged action.
One dose delivery.
It is easily absorbed from the injection site and penetrates into most organs and tissues of the animal.
The highest concentration of the antibiotic in blood is noted after 1 - 2 hours and is maintained at therapeutic level for at least 48 hours after parenteral administration of the drug.
Composition: Amoxicillin 15% LA contains amoxicillin trihydrate as an active ingredient, 150 mg in 1 ml, as well as excipients: colloidal silica, sorbitan monooleate, and medium chain triglycerides.
Description: Suspension of white to light yellow color. The suspension may separate into layers during storage, but should become homogenous after vial shaking. In the presence of water, a gelled sludge forms in the suspension.
Purpose: Amoxicillin 15% LA is prescribed for therapeutic purposes in cattle, sheep, pigs, dogs and cats for infectious diseases of the gastrointestinal tract, respiratory tract, urogenital system, joints, soft tissues and skin, necrobacillosis, umbilical infections, atrophic rhinitis, mastitis, metritis and agalactia syndrome, and other bacterial infections whose causative agents are sensitive to amoxicillin.
Contraindications: The animal's hypersensitivity to components of the drug and penicillin group antibiotics, as well as severe liver and/or kidney function disorders. Do not use the drug in any newborn animals, rabbits and guinea pigs.
Dosage and how to use: Amoxycillin 15% LA is administered to animals subcutaneously or intramuscularly once at a dose of 1 ml per 10 kg of animal weight (15 mg of active substance per 1 kg of animal weight). If re-injection of the drug is necessary, the 48-hour interval should not be exceeded, as this may lead to a decrease in therapeutic efficacy.
The maximum volume of the drug for administration in one place should not exceed 20 ml in cattle, 5 ml in pigs, sheep, calves, 2.5 ml in dogs, 1 ml in cats.
Withholding period: Slaughter of animals for meat is allowed not earlier than 28 days after the last administration of Amoxycillin 15% LA. Meat of animals slaughtered before the specified period may be used as feed for fur-bearing animals.
Milk may not be used for human consumption during drug administration and within 96 hours after the last injection. Milk obtained before the expiry of the milk withholding period can be boiled and fed to animals.
Storage life of Amoxycillin 15% LA in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.
- Gel
- Glycerin, carbomer, propylene glycol
- 250 ml
- Disinfectant
Suitable for all animal species as a ultrasound contact gel.
No contraindications.
Easy to remove, no rinsing required.
Ingredients: MIRALEK Ultra-Gel contains glycerin, carbomer, propylene glycol, acidity regulator, preservative, coloring agent, and purified water.
Description: Transparent jellylike mass of bluish color.
Purpose: MIRALEK Ultra-gel is used as a ultrasound contact gel for animals of all species.
Contraindications: None.
Dosage and how to use:
MIRALEK Ultra-gel is applied to the body surface of the animal in the area to be examined, in an amount sufficient for easy sliding of the transducer. Upon the completion of the ultrasound check, the gel is easily removed with a paper towel, and no rinsing is necessary.
Storage life of MIRALEK Ultra-gel, in the appropriate storage conditions in the closed original package: 3 years from the date of manufacture.
- Gel
- Glycerin, carbomer, propylene glycol
- 5 l
- Disinfectant
Suitable for all animal species as a ultrasound contact gel.
No contraindications.
Easy to remove, no rinsing required.
Ingredients: MIRALEK Ultra-Gel contains glycerin, carbomer, propylene glycol, acidity regulator, preservative, coloring agent, and purified water.
Description: Transparent jellylike mass of bluish color.
Purpose: MIRALEK Ultra-gel is used as a ultrasound contact gel for animals of all species.
Contraindications: None.
Dosage and how to use:
MIRALEK Ultra-gel is applied to the body surface of the animal in the area to be examined, in an amount sufficient for easy sliding of the transducer. Upon the completion of the ultrasound check, the gel is easily removed with a paper towel, and no rinsing is necessary.
Storage life of MIRALEK Ultra-gel, in the appropriate storage conditions in the closed original package: 3 years from the date of manufacture.
- Horses, cattle, pigs, sheep, goats, dogs, cats
- Antispasmodic agent
- Injectable solution
- 20 mg drotaverine hydrochloride per 1 ml of the drug
- 2 ml
An antispasmodic agent with myotropic action.
It does not have a stimulating effect on the respiratory system.
Easily absorbed from the injection site.
High concentration in blood plasma is achieved quickly (up to 98% binding to plasma proteins), the drug distributes evenly in tissues, and does not penetrate through the blood-brain barrier.
Ingredients: Spasmamiral contains drotaverine hydrochloride as an active ingredient, 20 mg per 1 ml, and excipients: disodium edetate dihydrate, benzethonium chloride, sodium disulfite, anhydrous sodium sulfite, sodium citrate pentasesquihydrate, ethanol, citric acid monohydrate, and water for injection.
Description: Clear liquid of light yellow to greenish-yellow color, opalescence is possible.
Purpose: Spasmamiral is used in horses, cattle, pigs, sheep, goats, dogs and cats to relieve spasms of smooth muscle in biliary tract diseases (cholangiolithiasis, cholecystitis, pericholecystitis, cholecystolithiasis, papillitis, cholangitis), urinary tract (pyelitis, cystitis, nephrolithiasis, urethrolithiasis, bladder tenesmus), gastrointestinal tract diseases (stomach and duodenal ulcer, gastritis, enteritis, colitis, cardiac and pylorus spasms), female reproductive system diseases.
Contraindications: The animal's hypersensitivity to the components of the drug, severe hepatic failure, renal failure, severe heart failure, glaucoma.
Dosage and administration:
Spasmamiral is administered 2 to 4 times a day intramuscularly or subcutaneously in the following dosages:
Horses: 0.6 - 0.8 mg per kg body weight (0.03 - 0.04 ml/kg).
For cattle: 0.6 - 0.8 mg per kg of body weight (0.03 - 0.04 ml/kg).
For pigs, sheep, goats: 0.8 - 1.0 mg per kg of body weight (0.04 - 0.05 ml/kg).
For dogs, cats: 1.0 - 1.5 mg per kg of body weight (0.05 - 0.075 ml/kg).
Withholding period: No withholding period is required for slaughter of animals for meat or the use of farm products.
Storage life of Spasmamiral in the appropriate storage conditions in the closed original package: 2 years from the date of production, 28 days after vial opening.
- Disinfectant
- Solution
- Sulfuric lime solution: 97.8%
- 100 ml
Disinfectant.
It is used to prevent or eliminate fungi and microscopic mites in places where animals are kept.
Effective antifungal and antiparasitic agent.
Composition: Lime Sulfur MIRALEK contains hydrogen sulfide lime, 97.8%, as well as inert ingredients.
Description: Concentrated solution of bright orange color with a pungent unpleasant odor; precipitation is possible. In this case, close the vial with the drug and immerse it in warm water for 20 minutes, after which use the product in accordance with the instructions.
Purpose: Lime Sulfur MIRALEK is a concentrated solution of hydrogen sulfide lime; it is used for the prevention and elimination of fungi and microscopic mites in animal housing.
Contraindications: Hypersensitivity to the drug.
Dosage and how to use: Lime Sulfur MIRALEK is diluted with water at a ratio of 1:32. The concentration of the drug may be doubled. Shake well before use! After adding the concentrate to the water, stir well. For chronic or resistant cases, the concentrate can be diluted as 8 ounces (226.8 ml) per 3.785 liters of water. Do not apply undiluted concentrated solution on the pet. The solution must be diluted according to the instructions. Apply the diluted concentrate to the skin area, do not rub it in. Do not rinse off after application. Wait until it dries completely. Do not use a hairdryer.
Storage life of Lime Sulfur MIRALEK in the appropriate storage conditions in the closed original package: 3 years from the date of manufacture.
- Cattle, dogs, cats
- Hepatoprotective agent
- Injectable solution
- 50 mg of phosphatidylcholine per 1 ml of the drug
- 5 ml
Promotes metabolism of lipids and proteins.
Improves the detoxifying function of the liver.
Helps to eliminate cholesterol from the body.
Ingredients: Hepamiral contains phosphatidylcholine as an active ingredient, 50 mg/1 ml, as well as excipients: deoxycholic acid, benzyl alcohol, sodium chloride, sodium hydroxide, riboflavin sodium phosphate, and water for injection.
Description: Transparent liquid of light yellow to yellow color, without visible mechanical inclusions.
Indications: Hepamiral is prescribed for cattle, dogs and cats as therapeutic and prophylactic agent in acute and chronic liver diseases (cirrhosis, hepatitis, hepatosis), as well as in gallbladder and biliary tract diseases of various genesis.
Contraindications: Hypersensitivity of the animal to the components of the drug.
The order of administration and dosage:
"Hepamiral" is administered intravenously in the following dosages:
20 - 25 ml per animal per day in cattle, in severe cases 35 - 40 ml per animal; the daily dose can be divided into 2 administrations.
Dogs and cats: 0.1 - 0.3 ml/kg body weight per day, in severe cases 0.5 - 0.6 ml/kg body weight.
Before use, the drug is diluted 1:1 with 5% or 10% glucose solution. For intravenous drip injection, the drug is diluted in 250 - 300 ml of 5% glucose solution and administered at a rate of 40 - 50 drops/min. The drug solution should remain clear during the entire time of administration.
The duration of a treatment course depends on the severity of the disease, but must not exceed 20 days.
Withholding period: No withholding period is required for slaughter of animals for meat.
Milk derived from lactating dairy cattle receiving the drug can be used for human consumption without any limitations.
Storage life of Hepamiral in the appropriate storage conditions in the closed original package: 3 years from the date of manufacture.
- Cattle, sheep, pigs, dogs, cats
- Antibacterial agent
- Injectable suspension
- 150 mg of amoxicillin trihydrate per 1 ml of the drug
- 10 ml
Antibacterial agent of prolonged action.
One dose delivery.
It is easily absorbed from the injection site and penetrates into most organs and tissues of the animal.
The highest concentration of the antibiotic in blood is noted after 1 - 2 hours and is maintained at therapeutic level for at least 48 hours after parenteral administration of the drug.
Composition: Amoxicillin 15% LA contains amoxicillin trihydrate as an active ingredient, 150 mg in 1 ml, as well as excipients: colloidal silica, sorbitan monooleate, and medium chain triglycerides.
Description: Suspension of white to light yellow color. The suspension may separate into layers during storage, but should become homogenous after vial shaking. In the presence of water, a gelled sludge forms in the suspension.
Purpose: Amoxicillin 15% LA is prescribed for therapeutic purposes in cattle, sheep, pigs, dogs and cats for infectious diseases of the gastrointestinal tract, respiratory tract, urogenital system, joints, soft tissues and skin, necrobacillosis, umbilical infections, atrophic rhinitis, mastitis, metritis and agalactia syndrome, and other bacterial infections whose causative agents are sensitive to amoxicillin.
Contraindications: The animal's hypersensitivity to components of the drug and penicillin group antibiotics, as well as severe liver and/or kidney function disorders. Do not use the drug in any newborn animals, rabbits and guinea pigs.
Dosage and how to use: Amoxycillin 15% LA is administered to animals subcutaneously or intramuscularly once at a dose of 1 ml per 10 kg of animal weight (15 mg of active substance per 1 kg of animal weight). If re-injection of the drug is necessary, the 48-hour interval should not be exceeded, as this may lead to a decrease in therapeutic efficacy.
The maximum volume of the drug for administration in one place should not exceed 20 ml in cattle, 5 ml in pigs, sheep, calves, 2.5 ml in dogs, 1 ml in cats.
Withholding period: Slaughter of animals for meat is allowed not earlier than 28 days after the last administration of Amoxycillin 15% LA. Meat of animals slaughtered before the specified period may be used as feed for fur-bearing animals.
Milk may not be used for human consumption during drug administration and within 96 hours after the last injection. Milk obtained before the expiry of the milk withholding period can be boiled and fed to animals.
Storage life of Amoxycillin 15% LA in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.
- Horses, cattle, pigs, sheep, goats, dogs
- Nonsteroidal anti-inflammatory drug
- Injectable solution
- 500 mg of sodium metamizole monohydrate per 1 ml of the drug
- 100 ml
Nonsteroidal anti-inflammatory drug.
Fast pain relief.
Easily absorbed from the injection site.
High concentrations in blood plasma are reached quickly.
Composition: Mirazmizol contains sodium metamizole monohydrate as an active ingredient, 500 mg in 1 ml, as well as water for injection.
Description: Transparent liquid from colorless to light yellow color.
Purpose: Miramisole is used in horses, cattle, sheep, pigs, goats, dogs and cats for neuralgias, febrile conditions, muscular and joint rheumatism, acute and chronic arthritis, acute gastric diseases (e.g., intestinal spasms, flatulence, catarrhal spasm, acute intestinal dilation), endometritis, mastitis, tendovaginitis, mastitis, metritis and agalactia syndrome in pigs.
Contraindications: Hypersensitivity to the active substance of the drug, suppression of hematopoiesis (cytostatic or infectious neutropenia, agranulocytosis), renal failure, liver failure, hereditary hemolytic anemia.
Dosage and how to use:
Miramisol is used 2 - 3 times a day for 3 to 5 days in the following dosage:
For cattle, sheep, or goats: intravenous or intramuscular administration of 20 - 40 mg/kg of body weight (0.04 - 0.08 ml/kg) every 8 - 12 hours.
Pigs: intramuscular administration of 15 to 50 mg/kg body weight (0.03 to 0.1 ml/kg) every 8 to 12 hours.
Horses: intravenous or intramuscular administration of 20 - 50 mg/kg of body weight (0.04 - 0.1 ml/kg) every 8 - 12 hours.
Dogs and cats: intravenous, intramuscular or subcutaneous administration of 20 - 25 mg per kg body weight (0.04 - 0.05 ml/kg) every 8 - 12 hours.
Withholding period: Slaughter of animals for meat is allowed not earlier than 12 days after the last administration of Metamizole. If slaughter is necessary before the specified time, the meat may be used to feed carnivorous animals.
Milk of cows, goats and sheep can be used for human consumption 4 days after the last administration of Metamizole. Milk obtained during treatment of animals with the drug and before the expiry of the specified period may be used to feed carnivorous animals.
Storage life of Miramisol in the appropriate storage conditions in the closed original package: 3 years from the date of production, 28 days after vial opening.