Rococlos Vet. injektionsvæske, emulsion

Ima dovoljenje za promet

Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
Porcine rotavirus A, strain OSU 6, Inactivated
Porcine rotavirus A, strain OSU 6, Inactivated
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Clostridium perfringens, type C, beta toxoid
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Clostridium perfringens, type C, beta toxoid
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Clostridium perfringens, type C, beta toxoid
Porcine rotavirus A, strain OSU 6, Inactivated
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Porcine rotavirus A, strain OSU 6, Inactivated
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
Clostridium perfringens, type C, beta toxoid

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Informacije o zdravilu

Ime zdravila:

Rococlos Vet. injektionsvæske, emulsion

Učinkovina:

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Ciljne živalske vrste:

Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

intramuskularna uporaba

Podatki o zdravilu

Učinkovina / Jakost:

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1.00

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1.00

Dose
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1.00

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Farmacevtska oblika:

Emulzija za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- Pig
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Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

Na voljo samo v Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian

Na voljo v:

Denmark

Opis ovojnine zdravila:

Na voljo samo v Danish
Na voljo samo v Danish
Na voljo samo v Danish
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Na voljo samo v Danish

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English French Italian Latvian Lithuanian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Salfarm Danmark A/S

Datum dovoljenja za promet z zdravilom:

19/12/2025

Proizvodna mesta, odgovorna za sproščanje serij:

Bioveta a.s.

Pristojni organ:

Danish Medicines Agency

Številka dovoljenja za promet z zdravilom:

72024

Datum spremembe statusa dovoljenja za promet:

19/12/2025

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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Danish (, INJEKTIONSVÆSKE, EMULSION)

Objavljeno na dan: 24/06/2026

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