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 Steer, heifer Sheep, calf, foal Young goat, lamb	2 g/100 kg b.w./day 1 g/50 kg b.w./day 0.5 g/25 kg b.w./day 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 presented for human consumption.

Packaging Type:

Presented in unboxed plastic jars of 0.1, 0.5, 1, 1.5 and 2.5 kg.