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 šķīdums injekcijām liellopiem, aitām, kazām un zirgiem
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:
- Food And Veterinary Service
Broj autorizacije:
- V/DCP/21/0039
Datum promjene statusa odobrenja:
Referentna država članica:
Broj postupka:
- ES/V/0389/001
Dotična država članica:
-
Hrvatska
Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na 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
Latvian (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.
Latvian (PDF)
Objavljeno na: 15/07/2024
Označivanje
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
Latvian (PDF)
Objavljeno na: 15/07/2024
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