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amino acids, B-complex vitamins and electrolytes

Nutritional
Indications:

As an aid in the supportive treatment of debilitated animals and for supportive treatment of severe diarrhea in cattle, swine and horses. Aminolean aids in counteracting the protein, electrolyte and vitamin loss associated with these conditions.

Mature Cattle, Horses & Swine : 2 mL/kg of body weight
Calves, Foals & Piglets : 5 mL/kg of body weight

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  • List No. Unit Package Case Size
    1AMI001 500mL 12
    1AMI025 950mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

ivermectin 1.87% w/w

Anti-Parasitic
Indications:

For the treatment of infections with internal parasites, including bots, in horses.

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  • List No. Unit Package Case Size
    1BIM007 12 x 6.42g 6
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

calcium borogluconate (equivalent to 19.1 mg/mL of calcium) 23.0% w/v, sodium hypophosphite (equivalent to 10.0 mg/mL of phosphorus) 2.85% w/v, magnesium chloride hexahydrate 4.5% w/v, dextrose monohydrate 15.0% w/v

Nutritional
Indications:

As an aid in the treatment of milk fever and other calcium, glucose, magnesium and phosphorus defiencies of cattle, sheep, horses and swine.

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  • List No. Unit Package Case Size
    1CAL013 500mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

didecyl dimethyl ammonium chloride 4.61% w/v n, alkyl dimethyl benzyl ammonium chloride 3.07% w/v

Disinfectants/ Antiseptic
Indications:

Broad Spectrum Germicidal Detergent and Deodorant Virucidal-Bactericidal-Fungicidal

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  • List No. Unit Package Case Size
    1CLI003 4L 4
    1CLI001 20L 1
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

dextrose monohydrate USP (equivalent to 500 mg per mL) 50% w/v

Nutritional
Indications:

As an aid in the treatment of glucose deficiencies in cattle, horses, sheep, swine and in the treatment of acetonemia (ketosis) in cattle and pregnancy disease in sheep.

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  • List No. Unit Package Case Size
    1DEX020 500mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

Each 1000 mL contains:sodium chloride 5.50 g, sodium acetate 3.00 g, calcium chloride 2H2O 0.40 g, magnesium chloride 6H2O 0.30 g, potassium acetate 1.00 g, sodium citrate 0.70 g, dextrose H2O 50.00 g.

Nutritional
Indications:

Balanced Electrolyte Solution. As an aid in the treatment of dehydration and electrolyte disturbances in cattle, horses, sheep and swine.

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  • List No. Unit Package Case Size
    1ELE007 1000mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

ivermectin 1.87% w/w

Anti-Parasitic
Indications:

For the treatment of infections with internal parasites, including bots, in horses.

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  • List No. Unit Package Case Size
    1EQU025 6.42g 6x(12x6.42g)
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

ivermectin 1.87% / praziquantel 14.03%

Anti-Parasitic
Indications:

Consult your veterinarian for assistance in the diagnosis, treatment and control of parasitism. Equimax (ivermectin/praziquantel) Paste is indicated for the treatment and control of the following parasites:

  • Tapeworms,
  • Large Strongyles (adults),
  • Small Strongyles (adults, including those resistant to some benzimidazole class compounds),
  • Small Strongyles (fourth-stage larvae),
  • Pinworms (adults and fourth-stage larvae),
  • Ascarids (adults and third- and fourth-stage larvae),
  • Hairworms (adults),
  • Large-mouth Stomach Worms (adults),
  • Bots (oral and gastric stages),
  • Lungworms (adults and fourth-stage larvae),
  • Intestinal Threadworms (adults)
  • Summer Sores and Dermatitis caused by Neck Threadworm.
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  • List No. Unit Package Case Size
    1EQU027P 6.42g 6x(12x6.42g)
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

Each 23.6 g single dose syringe contains the equivalent of 3.6 g pyrantel base sufficient to treat 544 kg horse

Anti-Parasitic
Indications:

For the treatment of infections with internal parasites.

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  • List No. Unit Package Case Size
    1EXO003 12x23.6g 3
    1EXO004 6x47.2g 3
    1EXO011 50x23.6g 1
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

Each millilitre of Flunazine* contains 50 mg flunixin equivalent to 83 mg of flunixin meglumine USP, 0.1 mg edetate disodium, 2.2 mg sodium formaldehyde sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol, 5.0 mg phenol as preservative, hydrochloric acid to adjust the pH and water for injection q.s.

Anti-Inflammatory
Indications:

HORSE : Flunazine® is recommended for the alleviation of inflammation and associated pain in musculoskeletal disorders in the horse.Flunazine* is also recommended for the alleviation of visceral pain associated with colic in the horse.

CATTLE : Flunazine® is indicated for the control of pyrexia associated with Bovine Respiratory Disease. Flunazine® is also indicated for the control of pyrexia and inflammation associated with endotoxemia. In clinical studies, flunixin meglumine injectable as an adjunct to antibiotic therapy with oxytetracycline has been demonstrated to control pyrexia associated bovine respiratory disease.

Horses : The recommended dose for musculoskeletal disorders is 1.1 mg per kg (1 mL/45 kg) of body weight once daily. Treatment may be given by intravenous or intramuscular injection and repeated for up to 5 days. Intravenous studies show onset of activity is within 2 hours. Peak response occurs between 12 and 16 hours and duration of activity is 24 to 36 hours following intravenous and intramuscular administration. The recommended dose for the alleviation of pain associated with equine colic is 1.1 mg per kg of body weight. Intravenous administration is recommended for prompt relief. Should colic symptoms recur, treatment may be repeated as necessary. Clinical studies show that pain symptoms were alleviated in 37% of treated horses within 15 minutes, and 74% within 30 minutes. The cause of colic should be determined and treated with concomitant therapy.

Cattle : The recommended dose for cattle is 2.2 mg/kg (2 mL/45 kg) given by slow intravenous administration once a day for up to 3 days. The total daily dose should not exceed 2.2 mg/kg of body weight. Avoid rapid intravenous administration of the drug. Twenty-four (24) hours after administration, check if animal is febrile. Readminister only if the fever is 104F (40C) or higher

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  • List No. Unit Package Case Size
    1FLU001 50mL 12
    1FLU002 100mL 12
    1FLU016 250mL 12
  • Withdrawal Period Milk : 

    Do not use in lactating or dry dairy cows 

    Withdrawal Period Meat

    Cattle - 6 days
    Do not use in calves to be processed for veal.
    Do not administer to horses that are to be slaughtered for food

abamectin 1% w/v

Nutritional
Indications:

Warm to body temperature prior to administration. For intravenous use only. Administer the contents or such amount as determined by a veterinarian. Discard unused portion

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  • List No. Unit Package Case Size
    1LAC001 1L 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

lidocaine hydrochloride 20 mg/mL. epinephrine 0.01 mg/mL

Sedative
Indications:

NOTE : The lowest possible concentration and dose should always be used. Inject slowly. Do not inject intravenously. Infiltration anaesthesia may be obtained by intramuscular or subcutaneous injection. The following dosages are given for 2% lidocaine hydrochloride and epinephrine.

Horse :
Volar nerve block ..... 5 - 10 mL
Low epidural (erect animal) ..... 5 - 12 mL
Infiltration ..... 2 - 50 mL

Cattle :
Low epidural (erect animal) ..... 5 mL
N. Cornualis block (dehorning) ..... 20 mL
Paravertebral (al each side) ..... 10 - 15 mL
(for last thoracic) ..... 20 mL
Inflitration ..... 5 - 100 mL

Calf :
Epidural ..... 3 - 10 mL

Sheep :
Epidural ..... 3 - 7 mL
Infiltration ..... 2 - 50 mL

Dog :
Epidural ..... 2 - 10 mL
Brachial Plexus Block (average size dog) ..... 10 mL
Infiltration ..... 2 - 10 ml

Cat :
Epidural ..... 0.5 - 2 mL
Infiltration ..... 0.5 - 4 mL.

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  • List No. Unit Package Case Size
    1LID009P 100mL 12
    1LID010P 250mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

    5 days

penicillin G procaine 300 000 IU/mL; preservative: methylparaben 0.1% w/v

Anti-Microbial
Indications:

Penicillin G Procaine Injectable Suspension USP

As an aid in the treatment of the following infections caused by bacteria susceptible to penicillin:

Cattle : Bacterial pneumonia, calf diphtheria, foot rot, metritis, wound infections.

Sheep : Bacterial pneumonia, metritis, wound infections.

Swine : Bacterial pneumonia, erysipelas, wound infections.

Horses : Bacterial pneumonia, metritis, strangles, wound infections.

DOSAGE : Shake well before using.

Cattle and Sheep : 21,000 IU/kg (7 mL/100 kg or 0.7 mL/10 kg) of body weight intramuscularly once daily until 2 days after clinical signs disappear. Do not exceed 5 days of treatment. Do not exceed 15 mL per injection site in cattle and 5 mL per injection site in sheep.

Swine : 15,000 IU/kg (1 mL/20 kg) of body weight intramuscularly once daily until 2 days after clinical signs disappear. Do not exceed 5 days of treatment. Do not exceed 10 mL per injection site.

Horses : 21,000 IU/kg (7 mL/100 kg) of body weight intramuscularly twice daily (at 12 hour intervals) until 2 days after clinical signs disappear or, in the case of respiratory infections, until 5 days after clinical signs disappear. Do not exceed 15 mL per injection site.

Rotate injection sites for succeeding doses.

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  • List No. Unit Package Case Size
    1PEN001 100mL 12
    1PEN002 250mL 12
    1PEN003 500mL 12
  • Withdrawal Period Milk : 

    96 hours

    Withdrawal Period Meat

    Cattle and Sheep - 10 days
    Swine - 8 days

Each 1000 mL contains: sodium chloride 9 g; water for injection q.s. milliequivalents: sodium 154 mEq/L; chloride 154 mEq/L; osmolarity 308 mOsmol/L; pH 4.5-7.0

Nutritional
Indications:

Warm to body temperature prior to administration. For intravenous use only. Dose and rate of administration will depend on the clinical condition of the patient. Administer as determined by a veterinarian.

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  • List No. Unit Package Case Size
    1PHY005 500mL 12
    1PHY006 1L 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

penicillin G procaine 300 000 IU/mL; preservative: methylparaben 0.1% w/v

Anti-Microbial
Indications:

Penicillin G Procaine Injectable Suspension USP

As an aid in the treatment of the following infections caused by bacteria susceptible to penicillin:

Cattle : Bacterial pneumonia, calf diphtheria, foot rot, metritis, wound infections.

Sheep : Bacterial pneumonia, metritis, wound infections.

Swine : Bacterial pneumonia, erysipelas, wound infections.

Horses : Bacterial pneumonia, metritis, strangles, wound infections.

DOSAGE : Shake well before using.

Cattle and Sheep : 21,000 IU/kg (7 mL/100 kg or 0.7 mL/10 kg) of body weight intramuscularly once daily until 2 days after clinical signs disappear. Do not exceed 5 days of treatment. Do not exceed 15 mL per injection site in cattle and 5 mL per injection site in sheep.

Swine : 15,000 IU/kg (1 mL/20 kg) of body weight intramuscularly once daily until 2 days after clinical signs disappear. Do not exceed 5 days of treatment. Do not exceed 10 mL per injection site.

Horses : 21,000 IU/kg (7 mL/100 kg) of body weight intramuscularly twice daily (at 12 hour intervals) until 2 days after clinical signs disappear or, in the case of respiratory infections, until 5 days after clinical signs disappear. Do not exceed 15 mL per injection site. Rotate injection sites for succeeding doses.

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  • List No. Unit Package Case Size
    1PRO056 100mL 12
    1PRO057 250mL 12
    1PRO058 500mL 12
  • Withdrawal Period Milk : 

    96 hours

    Withdrawal Period Meat

    Cattle and Sheep - 10 days
    Swine - 8 days

Each mL contains: sodium iodide 200 mg; preservatives: benzyl alcohol 0.25% w/v; methylparaben 0.03% w/v; propylparaben 0.025% w/v

Anti-Parasitic
Indications:

For the treatment of actinomycosis and actinobacillosis in cattle and as an expectorant in mild respiratory disease of cattle, horses and sheep.

DOSAGE: Administer by intravenous injection.

Cattle: Actinomycosis and actinobacillosis: 15 mL per 45 kg body weight. Repeat in 7-10 days.

Cattle, Horses and Sheep: As expectorant: 1 to 3 mL per 40 kg body weight. Repeat in 7-10 days if necessary.

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  • List No. Unit Package Case Size
    1SOD009 250mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

water for injection 100% v/v. non-pyrogenic

Nutritional
Indications:

Sterile Water USP is indicated for use as a sterile solvent or diluent for injectable solutions in such species as horses, cattle, swine, sheep, goats, dogs, cats, etc.

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  • List No. Unit Package Case Size
    1STE015 250mL 12
    1STE017 500mL 12
    1STE021 1L 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

A non-sterile solution containing 25 grams of sodium sulfamethazine in each 100 mL

Anti-Microbial
Indications:

Cattle & Sheep : As an aid in the treatment of the following conditions caused by bacteria sensitive to sulfamethazine: foot rot, shipping fever, bacterial enteritis/scours, metritis, mastitis, bacterial respiratory disease. As an aid in the treatment of coccidiosis in sheep.

Calves : As an aid in the treatment of the following conditions caused by bacteria sensitive to sulfamethazine: bacterial respiratory infections and secondary infections in bacterial enteritis/scours. As an aid in the prevention of coccidiosis.

Swine : As an aid in the treatment of bacterial enteritis, mastitis, metritis, and bacterial respiratory diseases caused by bacteria sensitive to sulfamethazine.

Horses : As an aid in the treatment of strangles, navel ill, joint ill (septic arthritis), bacterial enteritis and many secondary bacterial infections, associated with respiratory virus infections, caused by bacteria sensitive to sulfamethazine.

Poultry : As an aid in the treatment of caecal coccidiosis in chickens.

DOSAGE : For oral use.

Dairy Cattle, Calves, Sheep, Swine and Horses : First day: 45 mL of 25% sodium sulfamethazine for each 50 kg of body weight. Second and following days: one half of the above dosage. Do not treat for more than 5 days.

Beef Cattle : First day: for each 100 kg of body weight, add 100 mL of 25% of sodium sulfamethazine into the amount of water that will be consumed daily by the animal(s). Second and following days: one half of the above dosage. Do not treat for more than 5 days.

Poultry : Mix 35 mL of product per 9 litres of drinking water for 2 days - then reduce dosage to 17.5 mL of product per 9 litres of drinking water for 5 additional days. Allow access to medicated water only.

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  • List No. Unit Package Case Size
    1SUL002P 4L 12
  • Withdrawal Period Milk : 

    96 hours

    Withdrawal Period Meat

    12 days
    This product must not be added to swine feeds.

triamcinolone acetonide: 1.0 mg/g; nystatin 100 000 units/g; neomycin (as sulfate) 2.5 mg/g; gramicidin 0.25 mg/g

Anti-Microbial
Indications:

Apply a small quantity to affected area two or three times daily.

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  • List No. Unit Package Case Size
    1THE001P 15g 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat

xylazine HCl equivalent to 100 mg/mL xylazine base. preservatives: 0.9 mg/mL methylparaben and 0.1 mg/mL propylparaben.

Sedative
Indications:

Horses - Xylamax (xylazine HCl) Injection should be used when it is desirable to produce a state of sedation accompanied by a shorter period of analgesia. It has been successfully used when conducting various diagnostic, orthopaedic and dental procedures and for minor surgical procedures of short duration. It may also be used as a preanesthetic to local or general anesthesia.

Dosage and Administration:

Horses- For intravenous or intramuscular administration. Sedation and analgesia: The recommended dose for intravenous administration is 0.5 mL/45 kg body weight (equivalent to 1.1 mg/kg or 0.5 mg/lb). The recommended dose for intramuscular administration is 1.0 mL/45 kg of body weight (equivalent 2.2 mg/kg or 1.0 mg/lb).
Following the administration of Xylamax (Xylamax HCl) Injection, the animal should be allowed to rest quietly until the full effect has been reached. These dosages produce a state of sedation which is usually maintained for 1 to 2 hours and analgesia which lasts for 15 to 30 minutes.

Preanesthetic to local anesthesia - At the recommended dosage rates, Xylamax (Xylamax HCl) Injection may be used in conjunction with local anesthetics, such as procaine and lidocaine.

Preanesthetic to general anesthesia - At the recommended dosage rates, Xylamax (Xylamax HCl) Injection produces an additive effect to central nervous system depressants, such as sodium pentobarbital, sodium thiopental and sodium thiamylal. Accordingly, the dosage of such compounds should be reduced and administered to the desired effect. Generally, 1/3 to 1/2 of the calculated dosage of barbiturates will be needed to produce a surgical plane of anesthesia. Postanesthetic or emergence excitement has not been observed in animals preanesthetized with Xylazine HCl Injection.

Xylamax (Xylamax HCl) Injection has been successfully used as a preanesthetic agent with a dose range of 0.3 to 0.6 mg/kg prior to sodium pentobarbital, sodium thiopental, sodium thiamylal, nitrous oxide, ether, halothane, glyceryl guaiacolate or methoxyflurane anesthesia. Xylamax can be used at the full intravenous sedative dose (1.0 to 1.1 mg/kg) before ketamine HCl (Ketalean) induction.

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  • List No. Unit Package Case Size
    1XYL002 50mL 12
  • Withdrawal Period Milk : 

    Withdrawal Period Meat