ROMPERVAC 4+, suspensie injectabilă
ROMPERVAC 4+, suspensie injectabilă
Pooblaščeno
- Clostridium perfringens, serotype A, Inactivated
- Clostridium perfringens, serotype B, Inactivated
- Clostridium perfringens, serotype C, Inactivated
- Clostridium perfringens, serotype D, Inactivated
- Clostridium perfringens, type A and C, alpha toxoid
- Clostridium perfringens, type B, C and D, beta toxoid
- Clostridium perfringens, type B and D, epsilon toxoid
Identifikacija zdravila
Ime zdravila:
ROMPERVAC 4+, suspensie injectabilă
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English80.00Infectious unit(s)1.00millilitre(s)
-
Na voljo samo v English400.00Infectious unit(s)1.00millilitre(s)
-
Na voljo samo v English400.00Infectious unit(s)1.00millilitre(s)
-
Na voljo samo v English80.00Infectious unit(s)1.00millilitre(s)
-
Na voljo samo v English2.00international unit(s)1.00millilitre(s)
-
Na voljo samo v English10.00international unit(s)1.00millilitre(s)
-
Na voljo samo v English5.00international unit(s)1.00millilitre(s)
Farmacevtska oblika:
-
Suspenzija za injiciranje
Withdrawal period by route of administration:
-
Subkutana uporaba
- govedo
-
Milk0day
-
Meat and offal0day
-
- Sheep
-
Milk0day
-
Meat and offal0day
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QI02AB01
- QI04AB01
Pravni status za dobavo / izdajo zdravila:
Ta podatek za to zdravilo ni na voljo.
Status dovoljenja:
-
Valid
Available in:
-
Romania
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Pasteur Filiala Filipesti S.A.
Pristojni organ:
- Institute For Control Of Biological Products And Veterinary Medicines
Številka dovoljenja :
- 150404
Datum spremembe statusa dovoljenja:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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Romanian (PDF)
Objavljeno na: 25/05/2022
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