Neomar
Oral Solution Powder
Aminoglycosides group
Composition:
Each g contains 500 mg Neomycin sulphate equivalent to Neomycin base.
Indications:
In cattle, horses, sheep, hens, turkeys and ducks, used for the treatment of bacterial enteritis caused by bacteria susceptible to Neomycin.
Dose of Administration:
Unless recommended otherwise by the veterinarian;
Pharmacological dose:
In cattle, horses, steers, heifer, sheep, calves, foals, young goats and lambs 10 mg/kg.b.w/day
In poultry, 10-30 mg/kg b.w./day is added to the tap water and administered orally.
Practical dose:
| Animal Type | Dose |
| Cattle, horse | 2 g/100 kg b.w./day |
| Steer, heifer | 1 g/50 kg b.w./day |
| Sheep, calf, foal | 0.5 g/25 kg b.w./day |
| Young goat, lamb | 0.2 g/10 kg b.w./day |
| Animal Type | 10 mg/kg, the amount of Neomar that will be administered with pharmacological dose calculation | 20 mg/kg, the amount of Neomar that will be administered with pharmacological dose calculation | 30 mg/kg, the amount of Neomar that will be administered with pharmacological dose calculation |
| Hen, turkey, duck | 2 g/100 kg b.w./day | 4 g/100 kg b.w./day | 6 g/100 kg b.w./day |
Medicated water is prepared fresh daily. Treatment should continue in all types for 3-5 days.
Drug Residue Withdrawal Period (D.R.W.P):
Cattle, sheep, hens and turkeys should not be sent to slaughter during treatment or until 1 day after the last drug administration. Withdrawal period for poultry cows and sheep is “0” days. Eggs produced during treatment or within 1 days following the last drug administration should not be preseneted for human consumption.
Packaging Type:
Presented in unboxed plastic jars of 0.1, 0.5, 1, 1.5 and 2.5 kg.
