E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
Authorised
- ALPHA-TOCOPHEROL
- Sodium selenite
Auðkenning lyfsins
Heiti lyfs:
E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
E-SELENSOL 70/1 mg/ml, injekcinė emulsija galvijams, avims ir kiaulėms
Dýrategundir:
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Nautgripir
-
Svín
-
Sauðkind
Íkomuleið:
-
Til notkunar í vöðva
-
Til notkunar undir húð
Upplýsingar um lyfið
Lyfjaform:
-
Stungulyf, fleyti
Withdrawal period by route of administration:
-
Intramuscular use
- Nautgripir
-
Kjöt og innmatur14dagarNot authorised for use in animals producing milk for human consumption.
-
- Svín
-
Kjöt og innmatur14dagar
-
- Sauðkind
-
Kjöt og innmatur30dagarNot authorised for use in animals producing milk for human consumption.
-
-
Subcutaneous use
- Nautgripir
-
Kjöt og innmatur14dagarNot authorised for use in animals producing milk for human consumption.
-
- Svín
-
Kjöt og innmatur14dagar
-
- Sauðkind
-
Kjöt og innmatur30dagarNot authorised for use in animals producing milk for human consumption.
-
ATC flokkun (dýralyf):
- QA12CE99
Lögformleg staða:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Staða markaðsleyfis:
-
Gilt
Authorised in:
-
Litáen
Viðbótarupplýsingar
Entitlement type:
-
Markaðsleyfi
Lagagrundvöllur vöruleyfis:
- Aðeins í boði í English
Markaðsleyfishafi:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Labiana Life Sciences S.A.
Ábyrgt yfirvald:
- State Food And Veterinary Service
Markaðsleyfisnúmer:
- LT/2/21/2656/001-002
Dagsetning leyfisbreytingar:
Umsjónarland (RMS):
-
Ungverjaland
Númer verkferlis:
- HU/V/0143/001
Þátttökulönd (CMS):
-
Króatía
-
Kýpur
-
Eistland
-
Grikkland
-
Lettland
-
Litáen
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Skjöl
RV2656.pdf
Lithuanian (PDF)
Download Birt á: 23/05/2022
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