NEUROFISIN 10 I.U./ml ενέσιμο διάλυμα για ιπποειδή, βοοειδή, πρόβατα, αίγες, χοίρους, σκύλους, γάτες

Oprávnený

Oxytocin acetate

Download as PDF

Identifikácia lieku

Názov lieku:

NEUROFISIN 10 I.U./ml ενέσιμο διάλυμα για ιπποειδή, βοοειδή, πρόβατα, αίγες, χοίρους, σκύλους, γάτες

Účinná látka:

Dostupné len v English

Cieľové druhy:

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

Cesta podania:

Dostupné len v Spanish Greek English Portuguese
Subkutánne použitie

Podrobnosti o lieku

Účinná látka a sila:

Dostupné len v English

10.00

international unit(s)

/

1.00

millilitre(s)

Lieková forma:

Injekčný roztok

Withdrawal period by route of administration:

Intramuscular and intravenous use
- Horse
- Cattle
- Sheep
- Goat
- Pig
- Dog
- Cat
Subkutánne použitie
- Horse
- Cattle
- Sheep
- Goat
- Pig
- Dog
- Cat

Anatomicko-terapeuticko-chemický veterinárny kód (ATCvet):

QH01BB02

Právny stav dodávky:

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

Stav registrácie:

Valid

Authorised in:

Grécko

Available in:

Grécko

Opis balenia:

Dostupné len v Greek
Dostupné len v Greek
Dostupné len v Greek

Ďalšie informácie

Entitlement type:

Dostupné len v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Právny základ pre registráciu produktu:

Dostupné len v English

Držiteľ rozhodnutia o registrácii:

Fatro S.p.A.

Marketing authorisation date:

4/07/1995

Miesta výroby na uvoľnenie šarže:

Fatro S.p.A.

Zodpovedný orgán:

National Organization For Medicines

Číslo registrácie:

11014/05-07-1995/K-0141501

Dátum zmeny stavu registrácie:

5/10/2016

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

Ako užitočná bola táto stránka?: