Suivac APP emulsion for injection for pigs
Suivac APP emulsion for injection for pigs
Pooblaščeno
- Actinobacillus pleuropneumoniae, APX I toxoid
- Actinobacillus pleuropneumoniae, APX III toxoid
- Actinobacillus pleuropneumoniae, Inactivated
- Actinobacillus pleuropneumoniae, serotype 9, strain App9KL97, Inactivated
- Actinobacillus pleuropneumoniae, APX II toxoid
- Actinobacillus pleuropneumoniae, serotype 2, strain App2TR98, Inactivated
Identifikacija zdravila
Ime zdravila:
Suivac APP emulsion for injection for pigs
Suivac APP vet. injeksjonsvæske, emulsjon til svin.
Pot uporabe:
-
intramuskularna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1.00international unit(s)2.00millilitre(s)
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Na voljo samo v English1.00international unit(s)2.00millilitre(s)
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Na voljo samo v English1.00international unit(s)2.00millilitre(s)
-
Na voljo samo v English1.00international unit(s)2.00millilitre(s)
-
Na voljo samo v English1.00international unit(s)2.00millilitre(s)
-
Na voljo samo v English1.00international unit(s)2.00millilitre(s)
Farmacevtska oblika:
-
Emulzija za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- Pig
-
Meat and offal0day
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Meat and offal0day
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Meat and offal0day
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Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
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Meat and offal0day
-
Meat and offal0day
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QI09AB07
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Chemvet Dk A/S
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Dyntec spol. s r.o.
Pristojni organ:
- Norwegian Medical Products Agency
Številka dovoljenja :
- 16-11163
Datum spremembe statusa dovoljenja:
Številka postopka:
- DK/V/0119/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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Norwegian (PDF)
Objavljeno na: 27/01/2022
PI.pdf
English (PDF)
Prenesi Objavljeno na: 27/01/2022
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