ReVet RV 18

Oprávnený

Berberis vulgaris C4
LYTTA VESICATORIA C6
LYCOPODIUM CLAVATUM C9
Sabal serrulata C4

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Identifikácia lieku

Názov lieku:

ReVet RV 18

Účinná látka:

Dostupné len v English
Dostupné len v English
Dostupné len v English
Dostupné len v English

Cieľové druhy:

Dostupné len v Bulgarian Spanish Czech Danish German Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Slovenian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Slovenian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Slovenian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian English Latvian Lithuanian Hungarian Romanian Swedish
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Icelandic Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Norwegian
Dostupné len v Bulgarian Spanish Czech Danish Estonian English French Italian Latvian Lithuanian Hungarian Dutch Romanian Swedish Norwegian

Cesta podania:

Perorálne použitie

Podrobnosti o lieku

Účinná látka a sila:

Dostupné len v English

2.50

milligram(s)

/

1.00

gram(s)
Dostupné len v English

2.50

milligram(s)

/

1.00

gram(s)
Dostupné len v English

2.50

milligram(s)

/

1.00

gram(s)
Dostupné len v English

2.50

milligram(s)

/

1.00

gram(s)

Lieková forma:

Pilulky

Právny stav dodávky:

Dostupné len v Czech Estonian English French Italian Latvian Portuguese Slovenian Finnish Swedish Norwegian

Stav registrácie:

Valid

Authorised in:

Nemecko

Opis balenia:

Dostupné len v German
Dostupné len v German
Dostupné len v German
Dostupné len v German

Ďalšie informácie

Entitlement type:

Dostupné len v English French Italian Latvian Swedish Icelandic Norwegian

Držiteľ rozhodnutia o registrácii:

Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH

Marketing authorisation date:

10/03/2017

Zodpovedný orgán:

Číslo registrácie:

402335.00.00

Dátum zmeny stavu registrácie:

1/11/2021

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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