Versican Plus Pi/L4 (--) - Lyophilisate and suspension for suspension for injection
Versican Plus Pi/L4 (--) - Lyophilisate and suspension for suspension for injection
Viðurkennt
- Canine parainfluenza virus 2, strain CPiV-2-Bio 15, Live
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain MSLB 1089, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain MSLB 1090, Inactivated
- Leptospira kirschneri, serogroup Grippotyphosa, serovar Grippotyphosa, strain MSLB 1091, Inactivated
- Leptospira interrogans, serogroup Australis, serovar Bratislava, strain MSLB 1088, Inactivated
Auðkenning lyfsins
Upplýsingar um lyfið
Virkt efni / Styrkur:
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Aðeins í boði í EnglishPresentation_strength:10³·¹ - 10⁵·¹ TCID₅₀ Reference:Ph Eur 1955 Comments:Lyophilisate Index:0
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Aðeins í boði í EnglishPresentation_strength:≥ 1:51 ALR Reference:Ph Eur 0447 Comments:Suspension Index:1
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Aðeins í boði í EnglishPresentation_strength:≥ 1:51 ALR Reference:Ph Eur 0447 Comments:Suspension Index:2
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Aðeins í boði í EnglishPresentation_strength:≥ 1:40 ALR Reference:Ph Eur 0447 Comments:Suspension Index:3
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Aðeins í boði í EnglishPresentation_strength:≥ 1:51 ALR Reference:Ph Eur 0447 Comments:Suspension Index:4
Lyfjaform:
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Frostþurrkað stungulyf og dreifa, dreifa
Withdrawal period by route of administration:
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Til notkunar undir húð
- Hundur
ATC flokkun (dýralyf):
- QI07AI08
Lögformleg staða:
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Ávísunarskylt dýralyf
Staða markaðsleyfis:
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Gilt
Authorised in:
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Austurríki
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Belgía
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Búlgaría
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Króatía
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Kýpur
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Tékkland
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Danmörk
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Eistland
-
Finnland
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Frakkland
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Þýskaland
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Grikkland
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Ungverjaland
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Ísland
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Írland
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Ítalía
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Lettland
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Liechtenstein
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Litáen
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Lúxemborg
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Malta
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Holland
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Noregur
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Pólland
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Portúgal
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Rúmenía
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Slóvakía
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Slóvenía
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Spánn
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Svíþjóð
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Bretland (Norður-Írland)
Viðbótarupplýsingar
Entitlement type:
-
Marketing Authorisation
Markaðsleyfishafi:
- Zoetis Belgium SA
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Bioveta a.s.
Ábyrgt yfirvald:
- European Commission
Markaðsleyfisnúmer:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Dagsetning leyfisbreytingar:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Skjöl
Combined File of all Documents
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ema-puar-versican-plus-pi-l4-v-3683-par-en.pdf
English (PDF)
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