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 solução injetável para bovinos, suínos e ovinos
Djelatna tvar:
- Dostupno samo u English
Ciljne vrste životinja:
Način primjene:
-
Supkutano
-
Intramuskularno
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:
-
Supkutano
-
Cattle
-
Meat and offal22day
-
Milkno withdrawal periodMilk: 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
-
-
Cattle
-
Meat and offal22day
-
Milkno withdrawal periodMilk: 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
-
-
-
Intramuskularno
-
Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMilk: 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
-
-
Sheep
-
Meat and offal16day
-
Milkno withdrawal periodMilk: 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
-
-
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QJ01FA94
Status odobrenja:
-
Važeće
Available in:
-
Portugal
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
- Mevet S.A.
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- Mevet S.A.
Odgovorno tijelo:
- Directorate General For Food And Veterinary
Broj autorizacije:
- 1415/01/21DFVPT
Datum promjene statusa odobrenja:
Referentna država članica:
Broj postupka:
- ES/V/0393/001
Dotična država članica:
Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
Portuguese (PDF)
Objavljeno na: 8/10/2024
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
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
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