EURICAN DAP-LMULTI LYOPHILISATE AND SUSPENSION FOR SUSPENSION FOR INJECTION
EURICAN DAP-LMULTI LYOPHILISATE AND SUSPENSION FOR SUSPENSION FOR INJECTION
Pooblaščeno
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain 16069, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 16070, Inactivated
- Canine adenovirus 2, strain DK13, Live
- Canine distemper virus, strain BA5, Live
- Canine parvovirus, strain CAG2, Live
- Leptospira interrogans, serogroup Grippotyphosa, serovar Grippotyphosa, strain Grippo Mal 1540, Inactivated
Identifikacija zdravila
Ime zdravila:
EURICAN DAP-LMULTI LYOPHILISATE AND SUSPENSION FOR SUSPENSION FOR INJECTION
EURICAN DAP-L MULTI ΛΥΟΦΙΛΗ ΣΚΟΝΗ ΚΑΙ ΕΝΑΙΩΡΗΜΑ ΓΙΑ ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Pot uporabe:
-
Subkutana uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1.00Hamster protective Dose 80 % (Ph. Eur. Monograph)1.00millilitre(s)
-
Na voljo samo v English1.00Hamster protective Dose 80 % (Ph. Eur. Monograph)1.00millilitre(s)
-
Na voljo samo v English316.23tissue culture infective dose 501.00millilitre(s)
-
Na voljo samo v English10000.00tissue culture infective dose 501.00millilitre(s)
-
Na voljo samo v English79432.80tissue culture infective dose 501.00millilitre(s)
-
Na voljo samo v English1.00Hamster protective Dose 80 % (Ph. Eur. Monograph)1.00millilitre(s)
Farmacevtska oblika:
-
Liofilizat in suspenzija za suspenzijo za injiciranje
Withdrawal period by route of administration:
-
Subkutana uporaba
- Dog
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QI07AI03
Pravni status za dobavo / izdajo zdravila:
Ta podatek za to zdravilo ni na voljo.
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Boehringer Ingelheim Animal Health France
Pristojni organ:
- National Organization For Medicines
Številka dovoljenja :
- 105535/26-10-2020/K-0224701
Datum spremembe statusa dovoljenja:
Številka postopka:
- FR/V/0287/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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