NEOSKILAB Solution for injection
NEOSKILAB Solution for injection
Pooblaščeno
- NEOSTIGMINE METHYLSULFATE
Identifikacija zdravila
Ime zdravila:
NEOSKILAB Solution for injection
NEOSKILAB 1,5 mg/ml šķīdums injekcijām liellopiem, aitām, kazām un zirgiem
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1.50milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- govedo
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Sheep
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Goat
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Horse
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
-
Subkutana uporaba
- govedo
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Sheep
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Goat
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Horse
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QN07AA01
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Opis ovojnine:
- Na voljo samo v English
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Labiana Life Sciences S.A.
Pristojni organ:
- Food And Veterinary Service
Številka dovoljenja :
- V/DCP/21/0039
Datum spremembe statusa dovoljenja:
Številka postopka:
- ES/V/0389/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Povzetek glavnih značilnosti zdravila
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Navodilo za uporabo
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Latvian (PDF)
Objavljeno na: 23/05/2022
Označevanje
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
Latvian (PDF)
Objavljeno na: 23/05/2022
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