Šalis: Kanada
kalba: anglų
Šaltinis: Health Canada
TULATHROMYCIN
ALIVIRA ANIMAL HEALTH LIMITED
100MG
SOLUTION
TULATHROMYCIN 100MG
SUBCUTANEOUS
100
Prescription
CATTLE; CATTLE; CATTLE; CATTLE; SWINE (PIGS); SHEEP
Active ingredient group (AIG) number: 0151667001
APPROVED
2023-03-16
Dieline box Tulaject 250 ml 67 x 147 x 67 mm Dieline Varnish-free 147 mm 67 mm 67 mm TULAJECT Veterinary Use Only Antibiotic for cattle, swine and sheep PR TM DIN XXXXXXXX Sterile 100 mg of tulathromycin/mL Keep out of reach of children. NET: 250 ML WARNINGS: Treated animals must not be slaughtered for use in food for at least 44 days in cattle, 8 days in swine and 16 days in sheep, after the latest treatment with this drug. Do not use in dairy cows 20 months of age and older. To limit the development of antimicrobial resistance, Tulaject should only be used (1) as an arrival treatment in feedlot calves when BRD has been diagnosed and calves are at high risk of developing BRD, and (2) for control of SRD outbreak when groups of pigs are at high risk of developing SRD. Indications: _Beef and Non-lactating Dairy Cattle:_ For the treatment of bovine respiratory disease (BRD) and for the reduction of morbidity associated with BRD in feedlot calves during the first 14 days in the feedlot when administered at the time of arrival. For the treatment of infectious bovine keratocon- junctivitis (IBK). For the treatment of bovine foot rot (interdigital necrobacillosis). NOTE: To reduce the possibility of excess trim at the injection site it is recommended that swine not be slaughtered for up to 35 days after the latest treatment with this drug. Active Ingredient: Tulathromycin, 100 mg/mL Preservative: Monothioglycerol 5 mg/mL _Suckling Calves, Dairy Calves, and Veal _ _Calves:_ For the treatment of BRD. _Swine:_ For the treatment of swine respiratory disease (SRD) and for the control of SRD ingroups of pigs where SRD has been diagnosed. _Sheep:_ For the treatment of foot rot. See package insert for the complete list of bacteria susceptible to tulathromycin in cattle, swine and sheep. Dosage and Administration: Administer in the neck by subcutaneous injection in cattle and intramuscular injection in swine and sheep, a single dose of 2.5 mg/kg body weight. Do not inject more than 10 mL for cattle and 2.5 mL for swine and sheep Perskaitykite visą dokumentą