MASTICEN SECADO, intramaminė suspensija
MASTICEN SECADO, intramaminė suspensija
Odobreno
- Cloxacillin hemibenzathine
Identifikacija proizvoda
Naziv lijeka:
MASTICEN SECADO, intramaminė suspensija
Djelatna tvar:
- Dostupan samo u engleski
Ciljne vrste:
Put aplikacije:
-
Intramamarno
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupan samo u engleski1000.00/miligram1.00Štrcaljka
Farmaceutski oblik:
-
intramamarna suspenzija
Karencija prema putu aplikacije:
-
Intramamarno
-
Cattle (cow)
-
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-terapijsko-kemijska veterinarska (ATKvet) oznaka:
- QJ51CF02
Status odobrenja:
-
Važeće
Odobreno u:
- Dostupan samo u španjolski češki njemački estonski engleski francuski talijanski nizozemski portugalski slovački švedski islandski Norwegian
Dodatne informacije
Vrsta prava:
-
Marketing Authorisation
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
- Vetmarket UAB
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
- Cenavisa S.L.
Nadležno tijelo:
- State Food And Veterinary Service
Broj odobrenja:
- LT/2/02/1410/001-002
Datum promjene statusa odobrenja:
Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na www.adrreports.eu/vet
Dokumenti
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Objavljeno na: 23/12/2025
