Zantel Cat and Dog Tablets

Nazione: Irlanda

Lingua: inglese

Fonte: HPRA (Health Products Regulatory Authority)

Compra

Scarica Scheda tecnica (SPC)
12-06-2017
Scarica DSU (DSU)
30-08-2023

Principio attivo:

Praziquantel; Fenbendazole

Commercializzato da:

Chanelle Pharmaceuticals Manufacturing Limited

Codice ATC:

QP52AA51; QP52AC13

INN (Nome Internazionale):

Praziquantel; Fenbendazole

Dosaggio:

50/500 mg/tablet

Forma farmaceutica:

Tablet

Tipo di ricetta:

CAM: Companion Animal Medicine as defined in relevant national legislation

Gruppo terapeutico:

Cats, Dogs

Area terapeutica:

praziquantel, combinations; fenbendazole

Indicazioni terapeutiche:

Endoparasiticide

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2001-05-04

Scheda tecnica

                                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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