Veterinary Medicines

M+PAC

Authorised
  • Mycoplasma hyopneumoniae, Inactivated
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Auðkenning lyfsins

Heiti lyfs:
M+PAC
Virkt efni:
Dýrategundir:
  • Svín
Íkomuleið:
  • Til notkunar í vöðva

Upplýsingar um lyfið

Virkt efni / Styrkur:
  • Aðeins í boði í English
    1.47
    relative unit(s)
    /
    1.00
    millilitre(s)
Lyfjaform:
  • Stungulyf, fleyti
Withdrawal period by route of administration:
  • Intramuscular use
    • Svín
      • Kjöt og innmatur
        0
        dagar
ATC flokkun (dýralyf):
  • QI09AB13
Lögformleg staða:
Staða markaðsleyfis:
  • Gilt
Authorised in:
  • Lúxemborg
Áletrun:

Viðbótarupplýsingar

Entitlement type:
  • Markaðsleyfi
Lagagrundvöllur vöruleyfis:
Markaðsleyfishafi:
  • Intervet International B.V.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
  • Burgwedel Biotech GmbH
Ábyrgt yfirvald:
  • Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Markaðsleyfisnúmer:
  • V 817/02/08/0734
Dagsetning leyfisbreytingar:
Umsjónarland (RMS):
  • Ungverjaland
Númer verkferlis:
  • HU/V/0140/001/MR
Þátttökulönd (CMS):
  • Austurríki
  • Belgía
  • Kýpur
  • Tékkland
  • Danmörk
  • Eistland
  • Þýskaland
  • Grikkland
  • Írland
  • Ítalía
  • Lettland
  • Litáen
  • Lúxemborg
  • Pólland
  • Portúgal
  • Slóvakía
  • Slóvenía
  • Spánn
  • Svíþjóð
  • Bretland (Norður-Írland)
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