MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Ovlašten
- Marbofloxacin
Identifikacija proizvoda
Naziv VMP-a:
MARBOCYL 10% 100MG/1ML ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ
MARBOCYL 100 MG/ML, SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Djelatna tvar:
- Dostupno samo u English
Ciljne vrste životinja:
Način primjene:
-
Intramuskularno
-
Supkutano
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupno samo u English100.00miligram1.00mililitar
Farmaceutski oblik:
-
otopina za injekciju
Withdrawal period by route of administration:
-
Intramuskularno
-
Cattle
-
Meat and offal6dayIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC) -
Milk36satIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Meat and offal6dayIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Milk72satIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Meat and offal3dayIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Milk36satIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC)
-
-
Pig
-
Meat and offal4day
-
-
-
Supkutano
-
Cattle
-
Meat and offal6dayIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC) -
Milk36satIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Meat and offal6dayIndication : Mastitis
Dosage : 2mg/kg for 3 days (IV/IM/SC) -
Milk72satIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Meat and offal3dayIndication : Respiratory
Dosage : 8 mg/kg on a single occasion (IM) -
Milk36satIndication : Respiratory
Dosage : 2 m/kg for 3 to 5 days (IV/IM/SC)
-
-
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QJ01MA93
Status odobrenja:
-
Važeće
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
- Vetoquinol S.A.
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- VETOQUINOL BIOWET Sp. z o.o.
- Vetoquinol S.A.
Odgovorno tijelo:
- National Organization For Medicines
Broj autorizacije:
- 34664/13-05-2009/K-0130901
Datum promjene statusa odobrenja:
Broj postupka:
- FR/V/0107/001
Dotična država članica:
Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na www.adrreports.eu/vet
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