Flordofen 300 mg/ml Solution for injection for cattle and pigs
Flordofen 300 mg/ml Solution for injection for cattle and pigs
Authorised
- Florfenicol
Auðkenning lyfsins
Heiti lyfs:
Flordofen 300 mg/ml solution for injection for cattle and pigs
Flordofen 300 mg/ml Solution for injection for cattle and pigs
Virkt efni:
- Aðeins í boði í English
Dýrategundir:
-
Svín (til fitunar)
-
Nautgripir
Íkomuleið:
-
Til notkunar í vöðva
-
Til notkunar undir húð
Upplýsingar um lyfið
Virkt efni / Styrkur:
-
Aðeins í boði í English300.00milligram(s)1.00millilitre(s)
Lyfjaform:
-
Stungulyf, lausn
Withdrawal period by route of administration:
-
Intramuscular use
- Svín (til fitunar)
-
Kjöt og innmatur18dagar
-
- Nautgripir
-
Kjöt og innmatur30dagarMilk: Not authorised for use in animals producing milk for human consumption, including during the dry period.
-
-
Subcutaneous use
- Nautgripir
-
Kjöt og innmatur44dagarMilk: Not authorised for use in animals producing milk for human consumption, including during the dry period.
-
ATC flokkun (dýralyf):
- QJ01BA90
Staða markaðsleyfis:
-
Gilt
Authorised in:
-
Írland
Viðbótarupplýsingar
Entitlement type:
-
Markaðsleyfi
Markaðsleyfishafi:
- Dopharma Research B.V.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Dopharma B.V.
Ábyrgt yfirvald:
- Health Products Regulatory Authority
Markaðsleyfisnúmer:
- VPA10791/006/001
Dagsetning leyfisbreytingar:
Umsjónarland (RMS):
-
Portúgal
Númer verkferlis:
- PT/V/0112/001
Þátttökulönd (CMS):
-
Austurríki
-
Belgía
-
Búlgaría
-
Króatía
-
Tékkland
-
Danmörk
-
Eistland
-
Frakkland
-
Þýskaland
-
Grikkland
-
Ungverjaland
-
Írland
-
Ítalía
-
Lettland
-
Litáen
-
Holland
-
Pólland
-
Rúmenía
-
Slóvakía
-
Spánn
-
Bretland (Norður-Írland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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