Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
Ovlašten
- Tulathromycin
Identifikacija proizvoda
Naziv VMP-a:
Latroxin 100 mg/ml solution for injection for cattle, pigs and sheeps
LATROXIN 100 mg/ml, soluție injectabilă pentru bovine, porcine și ovine
Djelatna tvar:
- Dostupno samo u English
Ciljne vrste životinja:
Način primjene:
-
Intramuskularno
-
Supkutano
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupno samo u English100.00/miligram1.00mililitar
Farmaceutski oblik:
-
otopina za injekciju
Withdrawal period by route of administration:
-
Intramuskularno
- Cattle
-
Meat and offal22day
-
Milkno withdrawal periodMeat and offal: 22 days; Milk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
- Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMeat and offal: 16 days; Milk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
- Pig
-
Meat and offal13day
-
-
Supkutano
- Cattle
-
Meat and offal22day
-
Milkno withdrawal periodMeat and offal: 22 days; Milk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
- Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMeat and offal: 16 days; Milk: Not authorised for use in animals producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition
-
- Pig
-
Meat and offal13day
-
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QJ01FA94
Status odobrenja:
-
Važeće
Available in:
-
Romania
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
- Mevet S.A.U.
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- Mevet S.A.U.
Odgovorno tijelo:
- Institute For Control Of Biological Products And Veterinary Medicines
Broj autorizacije:
- 210058
Datum promjene statusa odobrenja:
Referentna država članica:
Broj postupka:
- ES/V/0393/001
Dotična država članica:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Sažetak opisa svojstava lijeka
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
English (PDF)
Objavljeno na: 12/04/2023
Romanian (PDF)
Objavljeno na: 21/02/2022
Uputa o lijeku
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
English (PDF)
Objavljeno na: 12/04/2023
Označivanje
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
English (PDF)
Objavljeno na: 12/04/2023
eu-PUAR-latroxin-100-mg-ml-solution-for-injection-for-cattle--pigs-and-sheeps-en.pdf
English (PDF)
Preuzimanje datoteka Objavljeno na: 12/04/2023
Koliko je bila korisna ova stranica?:
