NEOMAY 500 000 IU/G POWDER FOR USE IN DRINKING WATER/MILK

Nazione: Irlanda

Lingua: inglese

Fonte: HPRA (Health Products Regulatory Authority)

Compra

Scarica Scheda tecnica (SPC)
31-03-2017

Principio attivo:

NEOMYCIN (AS NEOMYCIN SULFATE)

Commercializzato da:

Laboratorios Maymó, S.A.

Codice ATC:

QA07AA01

INN (Nome Internazionale):

NEOMYCIN (AS NEOMYCIN SULFATE)

Dosaggio:

500 International Unit

Forma farmaceutica:

Powder for use in drinking water

Tipo di ricetta:

POM

Gruppo terapeutico:

Bovine, Fowl - Chicken, Fowl - Duck, Fowl, Fowl - Turkey, Porcine

Area terapeutica:

Neomycin

Indicazioni terapeutiche:

Antibacterial

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2016-12-23

Scheda tecnica

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
NEOMAY 500 000 IU/g powder for use in drinking water/milk
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Powder for use in drinking water/milk.
White or almost white powder.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle (calves), pigs (weaned and fattening pigs), chickens (including
layer hens), ducks, turkeys (including turkey
hens), geese, quail and partridges.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For treatment of gastrointestinal infections caused by E. coli
sensitive to neomycin.
4.3 CONTRAINDICATIONS
Do not use in case of hypersensitivity to the active substance, to
aminoglycosides or to the excipient.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Medicated drinking water intake can be affected by the severity of the
disease. In case of insufficient intake of water,
cattle and pigs should be treated parenterally.
Each g contains
ACTIVE SUBSTANCE:
Neomycin (as Neomycin sulphate)
500 000 IU
EXCIPIENTS:
For the full list of excipients, see section 6.1.
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4.5 SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
Powder for oral solution that is to be dissolved in water and cannot
be used as it is.
Special care should be taken when considering to administer the
product to 
                                
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