NexGard Spectra 18.75 mg + 3.75 mg - Chewable tablet
NexGard Spectra 18.75 mg + 3.75 mg - Chewable tablet
Viðurkennt
- Afoxolaner
- Milbemycin oxime
Auðkenning lyfsins
Upplýsingar um lyfið
Lyfjaform:
-
Tuggutafla
Withdrawal period by route of administration:
-
Til inntöku
- Hundur
ATC flokkun (dýralyf):
- QP54AB51
Lögformleg staða:
-
Ávísunarskylt dýralyf
Staða markaðsleyfis:
-
Gilt
Authorised in:
-
Austurríki
-
Belgía
-
Búlgaría
-
Króatía
-
Kýpur
-
Tékkland
-
Danmörk
-
Eistland
-
Finnland
-
Frakkland
-
Þýskaland
-
Grikkland
-
Ungverjaland
-
Ísland
-
Írland
-
Ítalía
-
Lettland
-
Liechtenstein
-
Litáen
-
Lúxemborg
-
Malta
-
Holland
-
Noregur
-
Pólland
-
Portúgal
-
Rúmenía
-
Slóvakía
-
Slóvenía
-
Spánn
-
Svíþjóð
-
Bretland (Norður-Írland)
Viðbótarupplýsingar
Entitlement type:
-
Marketing Authorisation
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)
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ema-puar-v3842-nexgard-spectra-ws2280-g-vra-0034-g-en.pdf
English (PDF)
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ema-puar-nexgard-spectra-v-3842-var-ii-0019-en.pdf
English (PDF)
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ema-puar-nexgard-spectra-v-3842-var-ii-0008-en.pdf
English (PDF)
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ema-puar-nexgard-spectra-nex-spe-var-ws1338-en.pdf
English (PDF)
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ema-puar-nexgard-spectra-v-3842-par-en.pdf
English (PDF)
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ema-puar-nexgard-spectra-nex-spe-var-ws1559-en.pdf
English (PDF)
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