Veterinary Medicines

Halagon 0.5 mg/ml - Oral solution

Authorised
  • Halofuginone
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Auðkenning lyfsins

Heiti lyfs:
Halagon 0.5 mg/ml - Oral solution
Virkt efni:
Dýrategundir:
  • Nautgripir (nýfæddur kálfur)
Íkomuleið:
  • Til inntöku

Upplýsingar um lyfið

Virkt efni / Styrkur:
  • Aðeins í boði í English
    0.50
    milligram(s)
    /
    1.00
    millilitre(s)
Lyfjaform:
  • Mixtúra, lausn
Withdrawal period by route of administration:
  • Oral use
    • Nautgripir (nýfæddur kálfur)
      • Kjöt og innmatur
        13
        dagar
ATC flokkun (dýralyf):
  • QP51AX08
Lögformleg staða:
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
Lagagrundvöllur vöruleyfis:
Markaðsleyfishafi:
  • Emdoka
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
  • Divasa Farmavic S.A.
Ábyrgt yfirvald:
  • European Commission
Markaðsleyfisnúmer:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Dagsetning leyfisbreytingar:

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