600000040779

Product identification

Názov lieku:

RABISIN vet, injeksjonsvæske, suspensjon Vaksine mot rabies til dyr (inaktivert)

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 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 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

Cesta podania:

Intramuskulárne použitie
Subkutánne použitie

Product details

Účinná látka a sila:

Dostupné len v English

2.09

log 10 optical density 50

/

1.00

international unit(s)

Lieková forma:

Injekčná suspenzia

Withdrawal period by route of administration:

Intramuskulárne použitie
- Horse
  - All relevant tissues
    
    0
    
    day
- Dog
- Cat
- Cattle
  - All relevant tissues
    
    0
    
    day
  - Milk
    
    0
    
    day
- Sheep
  - All relevant tissues
    
    0
    
    day
Subkutánne použitie
- Dog
- Cat
- Cattle
  - All relevant tissues
    
    0
    
    day
  - Milk
    
    0
    
    day
- Horse
  - All relevant tissues
    
    0
    
    day
- Sheep
  - All relevant tissues
    
    0
    
    day

Anatomicko-terapeuticko-chemický veterinárny kód (ATCvet):

QI07AA02

Právny stav dodávky:

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

Stav registrácie:

Valid

Authorised in:

Nórsko

Available in:

Nórsko

Opis balenia:

Dostupné len v Norwegian

Additional information

Entitlement type:

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

Právny základ pre registráciu produktu:

Dostupné len v English French Italian Latvian Norwegian

Držiteľ rozhodnutia o registrácii:

Boehringer Ingelheim Animal Health Denmark A/S

Marketing authorisation date:

22/10/2004

Miesta výroby na uvoľnenie šarže:

Boehringer Ingelheim Animal Health France SCS

Zodpovedný orgán:

Norwegian Medical Products Agency

Číslo registrácie:

1997-00851

Dátum zmeny stavu registrácie:

27/08/2009

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

Documents

Súhrn charakteristických vlastností lieku

Tento dokument v tomto jazyku (slovenčina) neexistuje. Nájdete ho v inom jazyku nižšie.

Ostatné jazyky (1)

Norwegian (PDF)

Publikované na: 27/06/2023

Updated on: 28/06/2023

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