Lactetrol Oplossing voor injectie
Lactetrol Oplossing voor injectie
Ovlašten
- Potassium chloride
- Sodium chloride
- Sodium lactate
- Calcium chloride dihydrate
- Magnesium chloride hexahydrate
Identifikacija proizvoda
Naziv VMP-a:
Lactetrol Oplossing voor injectie
Lactetrol Solution injectable
Lactetrol Injektionslösung
Ciljne vrste životinja:
Način primjene:
-
Intraperitonejski
-
Intravenski
-
Supkutano
Pojedinosti o proizvodu
Farmaceutski oblik:
-
otopina za injekciju
Withdrawal period by route of administration:
-
Intraperitonejski
- Sheep
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Cat
- Horse
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Pig
-
Meat and offalno withdrawal period0 days
-
- Goat
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Dog
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
-
Intravenski
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Horse
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Sheep
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Goat
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Pig
-
Meat and offalno withdrawal period0 days
-
- Dog
- Cat
-
Supkutano
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Horse
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Sheep
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Goat
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Pig
-
Meat and offalno withdrawal period0 days
-
- Cat
- Dog
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QB05XA30
Status odobrenja:
-
Važeće
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
- Dechra Veterinary Products
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- Eurovet Animal Health B.V.
Odgovorno tijelo:
- Federal Agency For Medicines And Health Products
Broj autorizacije:
- BE-V129184
Datum promjene statusa odobrenja:
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.
Dutch (PDF)
Objavljeno na: 22/03/2022
French (PDF)
Objavljeno na: 22/03/2022
Uputa o lijeku
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
Dutch (PDF)
Objavljeno na: 22/03/2022
French (PDF)
Objavljeno na: 22/03/2022
German (PDF)
Objavljeno na: 22/03/2022
Koliko je bila korisna ova stranica?: