ALGENAMIC 40 mg/ml solution for injection for cattle, pigs, dogs and cats
ALGENAMIC 40 mg/ml solution for injection for cattle, pigs, dogs and cats
Ima dovoljenje za promet
- Tolfenamic acid
Informacije o zdravilu
Ime zdravila:
ALGENAMIC 40 mg/ml solution for injection for cattle, pigs, dogs and cats
ALGENAMIC 40 mg/ml soluție injectabilă pentru bovine, porci, câiniși pisici
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Intravenska uporaba
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English40.00/milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Karenca glede na pot uporabe:
-
intramuskularna uporaba
-
govedo
-
Meat and offalno withdrawal periodMeat and offal: 12 days intramuscular use / 4 days intravenous use
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
Pig
-
Meat and offal16day
-
-
govedo
-
Meat and offalno withdrawal periodMeat and offal: 12 days intramuscular use / 4 days intravenous use
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
-
Intravenska uporaba
-
govedo
-
Meat and offalno withdrawal periodMeat and offal: 12 days intramuscular use / 4 days intravenous use
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
govedo
-
Meat and offalno withdrawal periodMeat and offal: 12 days intramuscular use / 4 days intravenous use
-
Milkno withdrawal periodMilk: Zero days intramuscular use/ 24 hours intravenous use
-
-
Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
- QM01AG02
Pravni status za dobavo/izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
-
Valid
Na voljo v:
-
Romania
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Vetpharma Animal Health S.L.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Mevet S.A.
Pristojni organ:
- Institute For Control Of Biological Products And Veterinary Medicines
Številka dovoljenja za promet z zdravilom:
- 210148
Datum spremembe statusa dovoljenja za promet:
Številka postopka:
- ES/V/0382/001
Zadevne države članice:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
Ta dokument ne obstaja v tem jeziku (slovenščina). Spodaj ga najdete v drugem jeziku.
