Tullavis

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PLEASE NOTE: A prescription issued by a UK registered vet (MRCVS) is required before this item can be dispatched.

Tullavis 100 mg/ml Injection

Available in 50ml & 100ml

Tullavis

PLEASE NOTE: A prescription issued by a UK registered vet (MRCVS) is required before this item can be dispatched.

Tullavis 100 mg/ml Injection

Product Description

Cattle

  • Treatment and metaphylaxis of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis susceptible to tulathromycin.
  • The presence of the disease in the herd should be established before metaphylactic treatment.
  • Treatment of infectious bovine keratoconjunctivitis (IBK) associated with Moraxella bovis susceptible to tulathromycin.

Pigs

  • Treatment and metaphylaxis of swine respiratory disease (SRD) associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Mycoplasma hyopneumoniae, Haemophilus parasuis and Bordetella bronchiseptica susceptible to tulathromycin.
  • The presence of the disease in the herd should be established before metaphylactic treatment.
  • The veterinary medicinal product should only be used if pigs are expected to develop the disease within 2–3 days.

Sheep

  • Treatment of the early stages of infectious pododermatitis (foot rot) associated with virulent Dichelobacter nodosus requiring systemic treatment.
Dosage & Administration

Cattle

  • Subcutaneous use.
  • A single subcutaneous injection of 2.5 mg tulathromycin/kg bodyweight (equivalent to 1 ml/40 kg bodyweight).
  • For treatment of cattle over 300 kg bodyweight, divide the dose so that no more than 7.5 ml are injected at one site.

Pigs

  • Intramuscular use.
  • A single intramuscular injection of 2.5 mg tulathromycin/kg bodyweight (equivalent to 1 ml/40 kg bodyweight) in the neck.
  • For treatment of pigs over 80 kg bodyweight, divide the dose so that no more than 2 ml are injected at one site.
  • For any respiratory disease, it is recommended to treat animals in the early stages of the disease and to evaluate the response to treatment within 48 hours after injection. If clinical signs of respiratory disease persist or increase, or if relapse occurs, treatment should be changed, using another antibiotic, and continued until clinical signs have resolved.

Sheep

  • Intramuscular use.
  • A single intramuscular injection of 2.5 mg tulathromycin/kg body weight (equivalent to 1 ml/40 kg body weight) in the neck.
Withdrawals

Cattle (meat and offal): 22 days.

Pigs (meat and offal): 13 days.

Sheep (meat and offal): 16 days.

Not authorised for use in animals producing milk for human consumption.

Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition.

You can download the datasheet here

You can visit the manufacturer’s website here

Available in 50ml & 100ml

milliliter

50ml, 100ml

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