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Liquid Injection

Title:

Nitroxynil injection 34%

Type:Liquid Injection
Release Date:2011/5/27 15:20:27
Inquiry:

 

 COMPOSITION:

Contains per ml:

Nitroxynil………………………………. 340 mg.

Solvents ad……………………………..1 ml.

DESCRIPTION:

Solution for injection. Clear, orange-red solution containing nitroxynil (as N-ethylglucamine salt) 34% w/v.

INDICATIONS:

It is indicated for the treatment of fascioliasis (infestations of mature and immature Fasciola hepatica) in cattle and sheep. It is also effective, at the recommended dose rate, against adult and larval infestations of Haemonchus contortus in cattle and sheep and Haemonchus placei, Oesophagostomum radiatum and Bunostomum phlebotomum in cattle. However, It should not be regarded or used as a broad spectrum anthelmintic.

DOSAGE AND ADMINISTRATION:

Administer by subcutaneous injection.

To ensure administration of a correct dose, body weight should be determined as accurately as possible; accuracy of the dosing device should be checked.

The standard dosage is 10mg nitroxynil per kilogram bodyweight.

Sheep: Administer according to the following doses scale:

 

Liveweight (kg)

Dose (ml)

14-20kg

0.5

21-30kg

0.75

31-40kg

1.0

41-55kg

1.5

56-75kg

2.0

Over 75kg

2.5

On farms with fluke-infested pastures, routine dosing should be carried out at intervals of not less than 49 days (7 weeks), having regard for such factors as the past disease history of the farm, the frequency and severity of neighbouring outbreaks and regional forecasts of incidence.

In outbreaks of acute fascioliasis advice on the best treatment should be sought from a veterinary surgeon.

Cattle: 1.5ml per 50kg (1cwt) liveweight.

Both infected and in-contact animals should be treated, treatment being repeated as considered necessary, though not more frequently than once per 60 days. The treatment of cattle helps reduce contamination of pastures on farms where fascioliasis is endemic or certain roundworm occurrence is evident.

CONTRAINDICATIONS:

For animal treatment only.

Do not use in animals with known hypersensitivity to the active ingredient.

Do not exceed stated dose.

WITHDRAWAL TIMES:

Cattle may be slaughtered for human consumption only after 60 days from the last treatment. Sheep may be slaughtered for human consumption only after 49 days from the last treatment. Not permitted for use in animals producing milk for human consumption, including pregnant animals intended to produce milk for human consumption.

PHARMACEUTICAL PRECAUTIONS:

Do not dilute or mix with other compounds.

Once the container has been broached, the contents should be used within 28 days.

This product does not contain a preservative.

Avoid the introduction of contamination. Should any apparent growth or discoloration occur, the product should be discarded.

Do not store above 25°C, protect from light.

Keep out of the reach and sight of children.

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.

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