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Veterinary Medicines

Porcilis AR-T DF (--) - Suspension for injection

Authorised
  • Pasteurella multocida, non-toxic derivative of dermonecrotic toxin, recombinant
  • Bordetella bronchiseptica, Inactivated

Auðkenning lyfsins

Heiti lyfs:
Porcilis AR-T DF (--) - Suspension for injection
Virkt efni:
Dýrategundir:
  • Svín (gylta)
  • Svín (gylta, óbyrja)
Íkomuleið:
  • Til notkunar í vöðva

Upplýsingar um lyfið

Virkt efni / Styrkur:
  • Aðeins í boði í English
    Presentation_strength:≥ 6.2 log2 TN. titre Reference:Hse Index:0
  • Aðeins í boði í English
    Presentation_strength:≥ 5.5 log2 Aggl.titre Reference:Hse Index:1
Lyfjaform:
  • Stungulyf, dreifa
Withdrawal period by route of administration:
  • Intramuscular use
    • Svín (gylta)
      • Á ekki við
        0
        dagar
    • Svín (gylta, óbyrja)
      • Á ekki við
        0
        dagar
ATC flokkun (dýralyf):
  • QI09AB04
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:
  • Intervet International B.V.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
  • INTERVET INTERNATIONAL B.V.
Ábyrgt yfirvald:
  • European Commission
Markaðsleyfisnúmer:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Dagsetning leyfisbreytingar:

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ema-puar-porcilis-ar-t-df-v-055-var-x-0009-en.pdf

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ema-puar-porcilis-ar-t-df-v-055-par-en.pdf

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