Propen 300 mg/ml Suspension for Injection for Cattle, Sheep and Pigs

Ima dovoljenje za promet

Benzylpenicillin procaine

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Informacije o zdravilu

Ime zdravila:

Propen 300 mg/ml Suspension for Injection for Cattle, Sheep and Pigs

Učinkovina:

Na voljo samo v English

Ciljne živalske vrste:

govedo
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Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

intramuskularna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

300.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Suspenzija za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Meat and offal
    
    7
    
    day
    
    For treatment duration of 3 days.
  - Meat and offal
    
    9
    
    day
    
    For treatment duration of 4-7 days.
  - Milk
    
    72
    
    hour
- Sheep
  - Meat and offal
    
    7
    
    day
    
    For a treatment duration of 3 days.
  - Meat and offal
    
    9
    
    day
    
    For a treatment duration of 4-7 days.
- Pig
  - Meat and offal
    
    7
    
    day
    
    For a treatment duration of 3 days.
  - Meat and offal
    
    9
    
    day
    
    For a treatment duration of 4-7 days.

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QJ01CE09

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Opis ovojnine zdravila:

Na voljo samo v English

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Interchem (Ireland) Limited

Datum dovoljenja za promet z zdravilom:

30/03/2012

Proizvodna mesta, odgovorna za sproščanje serij:

Interchem (Ireland) Limited

Pristojni organ:

Health Products Regulatory Authority

Številka dovoljenja za promet z zdravilom:

VPA10555/009/001

Datum spremembe statusa dovoljenja za promet:

30/03/2012

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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