
Tilmicosin Injection 30%
It is indicated for the treatment of respiratory infections in cattle and sheep associated with Mannheimia haemolytica, Pasteurella spp. and other tilmicosin-susceptible micro-organisms, and for the treatment of ovine mastitis associated with Staphylococcus aureus and Mycoplasma spp. Additional indications include the treatment of interdigital necrobacillosis in cattle.
Product Description
COMPOSITION
Contains per ml:
Tilmicosin base…………………………………. 300 mg
Solvents ad…………………………………………1 ml
INDICATIONS
It is indicated for the treatment of respiratory infections in cattle and sheep associated with Mannheimia haemolytica, Pasteurella spp. and other tilmicosin-susceptible micro-organisms, and for the treatment of ovine mastitis associated with Staphylococcus aureus and Mycoplasma spp. Additional indications include the treatment of interdigital necrobacillosis in cattle (bovine pododermatitis, foul in the foot) and ovine footrot.
USAGE AND DOSAGE
For subcutaneous injection
Cattle – pneumonia: 1 ml per 30 kg body weight (10 mg/kg).
Cattle – interdigital necrobacillosis: 0.5 ml per 30 kg body weight (5 mg/kg).
Sheep – pneumonia and mastitis: 1 ml per 30 kg body weight (10 mg/kg).
Sheep – footrot: 0.5 ml per 30 kg body weight (5 mg/kg).
CONTRA-INDICATIONS
Administration to equine, porcine or caprine species, or to lambs weighing 15 kg or less.
Administration to cattle producing milk for human consumption.
Do not use in heifers within 60 days of calving.
Do not use together with adrenalin or β-adrenergic antagonists such as propranolol.
WITHDRAWAL TIMES
For meat: Cattle: 60 days.
Sheep: 42 days.
For milk: Sheep: 15 days.
STORAGE PRECAUTIONS
Keep out of reach of children.
Protect from light and store in a cool dry place and below 30℃.