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Names of Products: 10% Enrofloxacin Injection
Publication date: 2015-12-24
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English Names: Enrofloxacin Injection
Components: Enrofloxacin

 

QUALITATIVE AND QUANTITATIVE COMPOSITION

Each ml contains:

Active substance:

Enrofloxacin               100mg

PHARMACEUTICAL FORM

Solution for injection.

Clear light yellow solution free from particulate matter.

Target species

Cattle and Pigs.

Indications for use, specifying the target species

Treatment of bacterial infections caused by strains susceptible to enrofloxacin.

Cattle:

Respiratory infections caused by Pasteurella spp. or Mycoplasma spp.

Alimentary tract infections caused by E. coli.

Treatment of local signs (inflammation, milk quality and yield) associated with peracute/acute mastitis in lactating dairy cattle caused by E. coli.

Pigs:

Respiratory infections caused by of Pasteurella spp. or Mycoplasma spp.

Alimentary tract infections caused by E. coli.

Enrofloxacin should be used where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice.

Amounts to be administered and administration route

To ensure correct dosage, body weight should be determined as accurately as possible to avoid underdosing.

Cattle:   

For respiratory and alimentary infections in cattle and secondary bacterial infections: administer by subcutaneous injection.

2.5 mg enrofloxacin per kg bodyweight daily by subcutaneous injection for 3 days (2.5 ml per 100 kg bodyweight). This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for complicated respiratory disease.

Not more than 10 ml should be administered at any one subcutaneous injection site.

For E. coli mastitis: administer by slow intravenous injection.

5.0 ml per 100 kg bodyweight (5 mg enrofloxacin per kg bodyweight) daily for 2 days.

Pigs:

For respiratory and alimentary infections in pigs and secondary bacterial infections: administer by intramuscular injection.

2.5 mg enrofloxacin per kg bodyweight daily by intramuscular injection for 3 days (2.5 ml per 100 kg bodyweight). This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for complicated respiratory disease.

Not more than 2.5 ml should be administered at any one intramuscular injection site.

Shelf life

Shelf-life of the veterinary medicinal product as packaged for sale: 3 years

Shelf-life after first opening the immediate packaging: 28 days.

Special precautions for storage

Do not store above 25oC.

After first opening the immediate packaging: do not store above 250C.

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