Animec 5 mg/ml Pour-on Solution for Cattle

Pajjiż: Irlanda

Lingwa: Ingliż

Sors: HPRA (Health Products Regulatory Authority)

Ixtrih issa

Ingredjent attiv:

Ivermectin

Disponibbli minn:

Chanelle Pharmaceuticals Manufacturing Limited

Kodiċi ATC:

QP54AA01

INN (Isem Internazzjonali):

Ivermectin

Dożaġġ:

5 milligram(s)/millilitre

Għamla farmaċewtika:

Pour-on solution

Tip ta 'preskrizzjoni:

POM: Prescription Only Medicine as defined in relevant national legislation

Żona terapewtika:

ivermectin

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2004-12-03

Karatteristiċi tal-prodott

                                Health Products Regulatory Authority
22 November 2018
CRN008PVZ
Page 1 of 6
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Animec 5 mg/ml Pour-on Solution for Cattle
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Active substance
Ivermectin 5 mg/ml
Excipients
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Pour-on solution.
A clear, slightly yellow coloured solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the effective treatment and control of the following species of
gastrointestinal
roundworms, lungworms, warbles, mites and lice:
GASTRO-INTESTINAL ROUNDWORMS (ADULTS AND FOURTH STAGE LARVAE)
_Ostertagia ostertagi_ (including inhibited _O. ostertagi_)
_Haemonchus placei_
_Trichostongylus axei _
_Trichostrongyulus colubiformis _
_Cooperia _spp
_Oesophagostomum radiatum _
_Strongyloides papillosus_ (adult)
_Trichuris spp_ (adult)
LUNGWORMS (ADULT AND FOURTH STAGE LARVAE):
_Dictyocaulus viviparus_
EYE WORMS (ADULT)
Health Products Regulatory Authority
22 November 2018
CRN008PVZ
Page 2 of 6
_Thelazia_ spp
WARBLES (PARASITIC STAGES):
_Hypoderma bovis_
_Hypoderma lineatum_
MITES:
_Chorioptes bovis_
_Sarcoptes scabiei_ var. _bovis._
SUCKING LICE:
_Linognathus vituli_
_Haematopinus eurysternus_
_Solenopotes capillatus_
BITING LICE
_Damalinia bovis_
Animec Pour-On given at the recommended dosage of 500 micrograms/kg
bodyweight, controls infections with _Trichostrongylus axei _and
_Cooperia _acquired up
to 14 days after treatment, _Ostertagia ostertagi_ and
_Oesophagostomum radiatum_
acquired during the first 21 days after treatment and _Dictyocaulus
viviparus_
(lungworm) acquired during the first 28 days after treatment.
It also controls horn flies (_Haematobia irritans_) for up 35 days
after treatment.
4.3 CONTRAINDICATIONS
Do not use in cases of known hypersensitivity to the active
ingredient. This product is
for application to skin surface only, do not give orally or
parenterally.
4.4 SPECIAL WARNINGS F
                                
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