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Veterinary Medicines

Prevomax 10 mg/ml - Solution for injection

Authorised
  • Maropitant

Auðkenning lyfsins

Heiti lyfs:
Prevomax 10 mg/ml - Solution for injection
Virkt efni:
Dýrategundir:
  • Hundur
  • Köttur
Íkomuleið:
  • Til notkunar í bláæð
  • Til notkunar undir húð
  • Til notkunar í bláæð
  • Til notkunar undir húð

Upplýsingar um lyfið

Virkt efni / Styrkur:
  • Aðeins í boði í English
    10.00
    milligram(s)
    /
    1.00
    Hettuglas
Lyfjaform:
  • Stungulyf, lausn
Withdrawal period by route of administration:
  • Intravenous use
    • Hundur
    • Köttur
  • Subcutaneous use
    • Hundur
    • Köttur
  • Intravenous use
    • Hundur
    • Köttur
  • Subcutaneous use
    • Hundur
    • Köttur
ATC flokkun (dýralyf):
  • QA04AD90
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
Áletrun:

Viðbótarupplýsingar

Entitlement type:
  • Markaðsleyfi
Markaðsleyfishafi:
  • Dechra Regulatory B.V
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
  • Produlab Pharma B.V.
  • Eurovet Animal Health B.V.
Ábyrgt yfirvald:
  • European Commission
Markaðsleyfisnúmer:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Dagsetning leyfisbreytingar:

Skjöl

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ema-puar-prevomax-v-4331-par-en.pdf

English (PDF)
Birt á: 15/03/2023
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