MASTICEN SECADO, intramaminė suspensija
MASTICEN SECADO, intramaminė suspensija
Ima dovoljenje za promet
- Cloxacillin hemibenzathine
Informacije o zdravilu
Ime zdravila:
MASTICEN SECADO, intramaminė suspensija
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
krava
Pot uporabe:
-
Intramamarno dajanje
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English1000.00/milligram(s)1.00Brizga
Farmacevtska oblika:
-
intramamarna suspenzija
Karenca glede na pot uporabe:
-
Intramamarno dajanje
-
krava
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Sheep
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Goat
-
Meat and offal0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dayIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
- QJ51CF02
Pravni status za dobavo/izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
-
Valid
Opis ovojnine zdravila:
- Na voljo samo v Lithuanian
- Na voljo samo v Lithuanian
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Vetmarket UAB
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Cenavisa S.L.
Pristojni organ:
- State Food And Veterinary Service
Številka dovoljenja za promet z zdravilom:
- LT/2/02/1410/001-002
Datum spremembe statusa dovoljenja za promet:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
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Lithuanian (PDF)
Objavljeno na dan: 23/12/2025
