CRIBENDAZOLE 10% 1L // ALBENDAZOLE

PRODUCT NAME 
CRIBENDAZOLE 10% 1L.

TARGET SPECIES: 
Cattle and sheep.

THERAPEUTIC INDICATIONS
Cribendazole suspension 10% is recommended for combating the following parasites in cattle and sheep:
Gastrointestinal strongylatosis produced by the genera Haemonchus, Ostertagia, Trichostrongylus, Nematodirus, Cooperia, Chabertia, Bunostomum, Oesophagostomum, Capillaria, Trichocephalus, as well as against Ascaris ovis and Neoascaris vitulorum;
Pulmonary strongylatosis produced by the genera Dictyocaulus, Protostrongylus, Mullerius, Cystocaulus, Neostrongylus, etc.;
Cestodoses produced by the adult forms of the genera Moniezia, Thysaniezia, Avitelina, located as adults in the intestine and in the muscular, visceral, serous cystic larval forms produced by Echinococcus granulosus, Taenia saginata, etc.;
Trematodes produced by the genera Fasciola (eggs and adults), Dicrocelium, Paramphistomum.
Albendazole is a very broad-spectrum endoparasiticide. Administered orally, it is quickly absorbed and diffuses in all organs and tissues, producing the lysis of worms, regardless of the species and category of the animals treated, as well as the location of the parasites, either at the level of the respiratory system, the digestive tract, the liver and various tissues. It is active against trematodes, cestodes and nematodes, in all their forms of evolution, respectively eggs, larvae, adults. The toxicity is reduced, the maximum tolerated doses being 5 times higher than the therapeutic ones. It is active against "Benzimidazole-resistant" strains of strongyles, such as Haemonchus and Trichostrongylus.

CONTRAINDICATIONS
There are none.

ADVERSE REACTIONS
If you notice other serious reactions or other effects that are not mentioned in this leaflet, please inform your veterinarian.

RECOMMENDATIONS REGARDING THE CORRECT ADMINISTRATION
The treatment is done orally, with a measuring cup (bottle), or with a syringe, into which the required amount of well-homogenized 10% Cribendazole suspension has been inserted.
The prophylaxis program must include 4 administrations annually, respectively: before leaving for grazing and after entering the stable and during grazing, in the months of July and September.
The live weight of the animals will be correctly estimated to avoid underdosing or overdosing.
In cattle, the dose is 7.5 ml suspension/100 kg live weight.
In sheep, the dose is 0.5 ml suspension/10 kg live weight.
In the case of fasciolosis, the doses are as follows:
In cattle, the dose is 10 ml suspension/100 kg live weight.
In sheep, the dose is 0.75 ml suspension/10 kg live weight.

SPECIAL WARNINGS
None.

WAITING PERIOD
Beef: 14 days from the last administration.
Sheep meat: 4 days after the last administration.
Milk: 3 days after the last administration.