Tulaject

Indication

Cattle: It is indicated for the treatment and prevention of bovine respiratory disease caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis that are sensitive to Tulathromycin. Before preventive treatment, the presence of the disease in the herd should be confirmed. It is also indicated for the treatment of infectious bovine keratoconjunctivitis caused by Moraxella bovis, which is sensitive to Tulathromycin.

Sheep: It is used for the treatment of early stages of infectious pododermatitis (foot rot) associated with virulent Dichelobacter nodosus, which requires systemic treatment

Product Description

Composition
Each ml contains 100 mg of Tulathromycin equivalent to 102.23 mg of Tulathromycin Monohydrate, and 5 mg of Monothioglycerol as an antioxidant preservative

Cattle: It is indicated for the treatment and prevention of bovine respiratory disease caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis that are sensitive to Tulathromycin. Before preventive treatment, the presence of the disease in the herd should be confirmed. It is also indicated for the treatment of infectious bovine keratoconjunctivitis caused by Moraxella bovis, which is sensitive to Tulathromycin.

Sheep: It is used for the treatment of early stages of infectious pododermatitis (foot rot) associated with virulent Dichelobacter nodosus, which requires systemic treatment

Cattle: The recommended dose is 2.5 mg/kg body weight/day via subcutaneous injection (1 ml/40 kg body weight). For cattle over 300 kg, the dose should be divided so that no more than 7.5 ml is applied to one area. Animals should be treated in the early stages of the disease, and results should be evaluated within 48 hours of administration.

Sheep: The recommended dose is 2.5 mg/kg body weight/day via intramuscular injection to the neck (1 ml/40 kg body weight). To prevent overdose or insufficient dose application, the animal’s body weight should be determined as accurately as possible before administration.

cattle, Sheep

Cattle should not be sent for slaughter within 22 days after drug administration, and sheep should not be sent for slaughter within 16 days. The drug should not be administered to lactating cows and sheep whose milk is used for human consumption, or to cows and sheep that are less than 2 months away from giving birth.

It is available for sale in colorless glass vials of 50 ml, 100 ml, and 250 ml, packaged in cardboard boxes

Alivira Türkiye
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