ACTI-TETRA I
ACTI-TETRA I
Ovlašten
- Oxytetracycline hydrochloride
Identifikacija proizvoda
Naziv VMP-a:
ACTI-TETRA I
Djelatna tvar:
- Dostupno samo u English
Ciljne vrste životinja:
Način primjene:
-
Intramuskularno
-
Supkutano
-
Intravenski
-
Intraperitonejski
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupno samo u English53.96miligram1.00mililitar
Farmaceutski oblik:
-
otopina za injekciju
Withdrawal period by route of administration:
-
Intramuskularno
- Cattle
-
Milk3day
-
Meat and offal14day
-
- Pig
-
Meat and offal14day
-
- Cat
- Horse
-
Milk3day
-
Meat and offal14day
-
- Sheep
-
Milk3day
-
Meat and offal14day
-
- Goat
-
Milk3day
-
Meat and offal14day
-
- Dog
-
Supkutano
- Cattle
-
Milk3day
-
Meat and offal14day
-
- Pig
-
Meat and offal14day
-
- Cat
- Horse
-
Milk3day
-
Meat and offal14day
-
- Sheep
-
Milk3day
-
Meat and offal14day
-
- Goat
-
Milk3day
-
Meat and offal14day
-
- Dog
-
Intravenski
- Cattle
-
Milk3day
-
Meat and offal14day
-
- Pig
-
Meat and offal14day
-
- Cat
- Horse
-
Milk3day
-
Meat and offal14day
-
- Sheep
-
Milk3day
-
Meat and offal14day.
-
- Goat
-
Milk3day
-
Meat and offal14day
-
- Dog
-
Intraperitonejski
- Cattle
-
Milk3day
-
Meat and offal14day
-
- Pig
-
Meat and offal14day
-
- Cat
- Horse
-
Milk3day
-
Meat and offal14day
-
- Sheep
-
Milk3day
-
Meat and offal14day
-
- Goat
-
Milk3day
-
Meat and offal14day
-
- Dog
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QJ01AA06
Status odobrenja:
-
Važeće
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
- Laboratoires Biove
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- Laboratoires Biové
Odgovorno tijelo:
- French Agency For Food, Environmental And Occupational Health & Safety
Broj autorizacije:
- FR/V/6090637 3/1988
Datum promjene statusa odobrenja:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Sažetak opisa svojstava lijeka
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French (PDF)
Objavljeno na: 4/04/2022
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