Porcilis Ery+Parvo+Lepto suspension for injection for pigs
Porcilis Ery+Parvo+Lepto suspension for injection for pigs
Pooblaščeno
- Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Leptospira interrogans, serogroup Canicola, serovar Portland-vere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Copenhageni, strain Ic-02-001, Inactivated
- Leptospira kirschneri, serogroup Grippotyphosa, serovar Dadas, strain GR-01-005, Inactivated
- Leptospira interrogans, serogroup Pomona, serovar Pomona, strain Po-01-000, Inactivated
- Leptospira santarosai, Serogroup Tarassovi, serovar Gatuni, strain S1148/02, Inactivated
- Leptospira interrogans, serogroup Australis, serovar Bratislava, strain As-05-073, Inactivated
Identifikacija zdravila
Ime zdravila:
Porcilis Ery+Parvo+Lepto suspension for injection for pigs
PORCILIS ERY + PARVO + LEPTO
Pot uporabe:
-
intramuskularna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1.00Protective Dose2.00millilitre(s)
-
Na voljo samo v English130.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English2816.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English210.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English648.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English166.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English276.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Na voljo samo v English1310.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
Farmacevtska oblika:
-
Suspenzija za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- Pig
-
Meat and offal0day
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QI09AL07
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Intervet International B.V.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- INTERVET INTERNATIONAL B.V.
Pristojni organ:
- Ministry Of Health
Številka dovoljenja :
- 104943
Datum spremembe statusa dovoljenja:
Številka postopka:
- DE/V/0268/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
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Italian (PDF)
Objavljeno na: 29/01/2024
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