Composition :
Each mL contains
Tulathromycin 100 mg
Excipients Up to 1 mL
Product Description :
TULAXINE Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass triamilide.
TULAXINE consists of an equilibrated mixture of two isomeric forms of tulathromycin in a 9:1 ratio.
Indications:
Beef and Non-Lactating Dairy Cattle
BRD – TULAXINE Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis.
and for the control of respiratory disease in cattle at high risk of developing BRD caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni,
and Mycoplasma bovis.
IBK – TULAXINE Injectable Solution is indicated for the treatment of infectious bovine keratoconjunctivitis (IBK) caused by Moraxella bovis.
Foot Rot – TULAXINE Injectable Solution is indicated for the treatment of bovine foot rot (interdigital necrobacillosis) caused by Fusobacterium necrophorum and Porphyromonas levii.
Suckling Calves, Dairy Calves, and Veal Calves
BRD – TULAXINE Injectable Solution is indicated for the treatment of BRD caused by M. haemolytica, P. multocida, H. somni, and M. bovis.
Swine
TULAXINE Injectable Solution is indicated for the treatment of swine respiratory disease (SRD) caused by Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica, Haemophilus parasuis, and Mycoplasma hyopneumoniae; and for the control of SRD caused by Actinobacillus pleuropneumoniae, Pasteurella multocida, and Mycoplasma hyopneumoniae in groups of pigs where SRD has been diagnosed.
DOSAGE:
Cattle: Inject subcutaneously as a single dose in the neck at a dosage of 2.5 mg/kg (1.1 mL/100 lb) body weight (BW) .
Do not inject more than 10 mL per injection site.
Swine: Inject intramuscularly as a single dose in the neck at a dosage of 2.5 mg/kg (0.25 mL/22lb) BW. Do not inject more than 2.5 mL per injection site.
Contraindications :
Do not use in case of hypersensitivity of the target animals to macrolide antibiotics.
Do not use simultaneously with other macrolides or lincosamides.
Do not use in lactating 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.
Target species:
cattle, pigs and sheep
Withdrawal periods:
Cattle (meat and offal): 22 days.
Pigs (meat and offal): 13 days.
Sheep (meat and offal): 16 days.
Presentation:
50 ml multi-dose vial, packed in single box.
Storage conditions:
Keep out of the sight and reach of children.
Store at or below 77°F (25°C) with excursions between 59-86°F (15-30°C).