Purevax RCPCh FeLV (--) - Lyophilisate and solvent for suspension for injection
Purevax RCPCh FeLV (--) - Lyophilisate and solvent for suspension for injection
Viðurkennt
- Feline calicivirus, strains 431 and G1, Inactivated
- Chlamydia felis, strain 905, Live
- Feline panleucopenia virus, strain PLI IV, Live
- Feline rhinotracheitis virus, strain F2, Live
- Canarypox virus, strain vCP97, expressing env and gag genes and a portion of the pol gene of Feline leukemia virus, Live
Auðkenning lyfsins
Upplýsingar um lyfið
Virkt efni / Styrkur:
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Aðeins í boði í EnglishPresentation_strength:≥2.0 ELISA U Reference:Hse Comments:Freeze dried pellet Index:0
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Aðeins í boði í EnglishPresentation_strength:≥10³·° EID₅₀ Reference:Hse Comments:Freeze dried pellet Index:1
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Aðeins í boði í EnglishPresentation_strength:≥10³·⁵ CCID₅₀ Reference:Hse Comments:Freeze dried pellet Index:2
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Aðeins í boði í EnglishPresentation_strength:≥10⁴·⁹ CCID₅₀ Reference:Hse Comments:Freeze dried pellet Index:3
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Aðeins í boði í EnglishPresentation_strength:≥10⁷·² CCID₅₀ Reference:Hse Comments:Diluent Index:4
Lyfjaform:
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Frostþurrkað stungulyf og leysir, dreifa
Withdrawal period by route of administration:
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Til notkunar undir húð
- Köttur
ATC flokkun (dýralyf):
- QI06AX
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
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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:
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Marketing Authorisation
Lagagrundvöllur vöruleyfis:
- Aðeins í boði í English
Markaðsleyfishafi:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Boehringer Ingelheim Animal Health France
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
íslenzkan (PDF)
Download Birt á: 20/04/2023
Bulgarian (PDF)
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Croatian (PDF)
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Czech (PDF)
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Danish (PDF)
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Dutch (PDF)
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English (PDF)
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Estonian (PDF)
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Finnish (PDF)
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French (PDF)
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German (PDF)
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Greek (PDF)
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Hungarian (PDF)
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Italian (PDF)
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Latvian (PDF)
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Lithuanian (PDF)
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Maltese (PDF)
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Norwegian (PDF)
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Polish (PDF)
Birt á: 20/04/2023
Portuguese (PDF)
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Romanian (PDF)
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Slovak (PDF)
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Slovenian (PDF)
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Spanish (PDF)
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Swedish (PDF)
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ema-puar-purevax-rcpch-felv-v-085-par-en.pdf
English (PDF)
Download Birt á: 15/03/2023
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