Zantel Cat and Dog Tablets

Šalis: Airija

kalba: anglų

Šaltinis: HPRA (Health Products Regulatory Authority)

Nusipirk tai dabar

Parsisiųsti Prekės savybės (SPC)
12-06-2017
Parsisiųsti DSU (DSU)
30-08-2023

Veiklioji medžiaga:

Praziquantel; Fenbendazole

Prieinama:

Chanelle Pharmaceuticals Manufacturing Limited

ATC kodas:

QP52AA51; QP52AC13

INN (Tarptautinis Pavadinimas):

Praziquantel; Fenbendazole

Dozė:

50/500 mg/tablet

Vaisto forma:

Tablet

Recepto tipas:

CAM: Companion Animal Medicine as defined in relevant national legislation

Farmakoterapinė grupė:

Cats, Dogs

Gydymo sritis:

praziquantel, combinations; fenbendazole

Terapinės indikacijos:

Endoparasiticide

Autorizacija statusas:

Authorised

Leidimo data:

2001-05-04

Prekės savybės

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Zantel Cat and Dog Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Tablet.
A round buff-coloured tablet with a quarter score.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs and cats
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
A broad spectrum anthelmintic for the treatment of mixed infections of
gastrointestinal nematodes and cestodes in dogs and
cats.
Zantel Cat and Dog tablets may also be used as an aid in the control
of_ Giardia_ protozoa in dogs and_ Aelurostrongylus_
_abstrusus_ lungworm infection in cats.
4.3 CONTRAINDICATIONS
Do not use in kittens less than 8 weeks of age.
ACTIVE SUBSTANCES (PER TABLET):
Praziquantel
50.0 mg
Fenbendazole
500.0 mg
Ascarids
_Toxocara cati (adult)_
_Toxascaris leonina (immature, adult)_
Hookworms
_Uncinaria stenocephala (immature, adult)_
_Ancylostoma caninum (immature, adult)_
Whipworms
_Trichuris vulpis (adult)_
Tapeworms
_Echinococcus granulosus_
_Echinococcus multilocularis_
_Dipylidium caninum_
_Taenia spp._
_Mesocestoides spp_
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4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
None.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL PRODUC
                                
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