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Names of Products: 30% Florfenicol Injection
Publication date: 2015-12-24
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English Names: Florfenicol Injection
Components: Florfenicol

 

QUALITATIVE AND QUANTITATIVE COMPOSITION

Each ml contains

Active substance:

Florfenicol                    300 mg

PHARMACEUTICAL FORM

Solution for injection

Clear slightly yellowish solution

Target species

Cattle and pigs

Indications for use, specifying target species

Cattle:

Prevention and treatment of respiratory tract infections in cattle due to Mannheimia haemolytica, Pasteurella multocida and Histophilus somni, susceptible to florfenicol.

The presence of the disease in the herd should be established before preventive treatment.

Pigs:

Treatment of acute outbreaks of respiratory disease caused by strains of Actinobacillus pleuropneumoniae and Pasteurella multocida susceptible to florfenicol.

Amounts to be administered and administration route

Cattle: Intramuscular or subcutaneous injection

Pigs: Intramuscular injection

Cattle:

Treatment

IM route: 20 mg florfenicol / kg bodyweight (1ml of the product/15kg) to be administered twice 48 hours apart using a 16 gauge needle.

SC route: 40 mg florfenicol / kg bodyweight (2ml of the product/15kg) to be administered once only using a 16 gauge needle.

Prevention

SC route: 40 mg florfenicol /kg bodyweight (2ml of the product/15kg) to be administered once only using a 16 gauge needle.

Pig:

15 mg florfenicol /kg bodyweight (1 ml of the product/ 20 kg) by intramuscular injection twice at 48 hour intervals using a 16-gauge needle.

The dose volume given at any one injection site should not exceed 10ml for both routes of administration (intramuscular and subcutaneous) in cattle and 3 ml in pigs. The injection should only be given in the neck in both target species.

To ensure a correct dosage body weight of the animals should be determined as accurately as possible to avoid underdosing.

It is recommended to treat animals in the early stages of disease and to evalsuate the response to treatment within 48 hours after the second injection. If clinical signs of respiratory disease persist 48 hours after the last injection or if relapse occurs, treatment should be changed using another formulation or another antibiotic and continued until clinical signs have resolved.

Swab septum before removing each dose. Use a dry sterile needle and syringe.

Do not broach the stopper of vial more than 25 times.

Shelf life

Shelf-life of the veterinary medicinal product as packaged for sale: 2 years

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

Special precautions for storage

Keep the vial in the outer carton in order to protect from light.

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