NEOSKILAB Solution for injection
NEOSKILAB Solution for injection
Ovlašten
- NEOSTIGMINE METHYLSULFATE
Identifikacija proizvoda
Naziv VMP-a:
NEOSKILAB Solution for injection
Neoskilab, 1,5 mg/ml süstelahus veistele, lammastele, kitsedele ja hobustele
Djelatna tvar:
- Dostupno samo u English
Ciljne vrste životinja:
Način primjene:
-
Intramuskularno
-
Supkutano
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupno samo u English1.50miligram1.00mililitar
Farmaceutski oblik:
-
otopina za injekciju
Withdrawal period by route of administration:
-
Intramuskularno
- Cattle
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Sheep
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Goat
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Horse
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
-
Supkutano
- Cattle
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Sheep
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Goat
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
- Horse
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Milkno withdrawal periodwithdrawal period is 0 days
-
Kod anatomsko-terapijsko-kemijske klasifikacije (ATKvet kȏd):
- QN07AA01
Status odobrenja:
-
Važeće
Opis paketa:
- Dostupno samo u English
Dodatne informacije
Entitlement type:
-
Marketing Authorisation
Nositelj odobrenja za stavljanje u promet:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Mjesta proizvodnje za izdavanje serije:
- Labiana Life Sciences S.A.
Odgovorno tijelo:
- State Agency Of Medicines
Broj autorizacije:
- 2299
Datum promjene statusa odobrenja:
Referentna država članica:
Broj postupka:
- ES/V/0389/001
Dotična država članica:
-
Hrvatska
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Sažetak opisa svojstava lijeka
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English (PDF)
Objavljeno na: 12/04/2023
Estonian (PDF)
Objavljeno na: 1/03/2022
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