Cardalis 5 mg benazepril hydrochloride + 40 mg spironolactone - Chewable Tablet
Cardalis 5 mg benazepril hydrochloride + 40 mg spironolactone - Chewable Tablet
Authorised
- Benazepril hydrochloride
- Spironolactone
Auðkenning lyfsins
Upplýsingar um lyfið
Lyfjaform:
-
Tuggutafla
Withdrawal period by route of administration:
-
Oral use
- Hundur
ATC flokkun (dýralyf):
- QC09BA07
Staða markaðsleyfis:
-
Gilt
Authorised in:
-
Austurríki
-
Belgía
-
Bretland (Norður-Írland)
-
Búlgaría
-
Danmörk
-
Eistland
-
Finnland
-
Frakkland
-
Grikkland
-
Holland
-
Króatía
-
Kýpur
-
Lettland
-
Liechtenstein
-
Litáen
-
Lúxemborg
-
Malta
-
Noregur
-
Portúgal
-
Pólland
-
Rúmenía
-
Slóvakía
-
Slóvenía
-
Spánn
-
Svíþjóð
-
Tékkland
-
Ungverjaland
-
Írland
-
Ísland
-
Ítalía
-
Þýskaland
Viðbótarupplýsingar
Entitlement type:
-
Markaðsleyfi
Markaðsleyfishafi:
- CEVA Santé Animale
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Catalent Germany Schorndorf GmbH
- Ceva Sante Animale
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-cardalis-v-2524-par-en.pdf
English (PDF)
Download Birt á: 17/03/2023
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