Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Odobreno
- Pentobarbital sodium
Identifikacija proizvoda
Naziv lijeka:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Djelatna tvar:
- Dostupan samo u engleski
Ciljne vrste:
Put aplikacije:
-
Intrakardijalno
-
Intravenski
-
Intraperitonejski
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupan samo u engleski400.00/miligram1.00mililitar
Farmaceutski oblik:
-
otopina za injekciju
Karencija prema putu aplikacije:
-
Intrakardijalno
-
Cattle
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Horse
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Pig
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
-
Intravenski
-
Cattle
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Horse
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Pig
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
-
Intraperitonejski
-
Cattle
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Horse
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Pig
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Anatomsko-terapijsko-kemijska veterinarska (ATKvet) oznaka:
- QN51AA01
Status odobrenja:
-
Važeće
Odobreno u:
- Dostupan samo u španjolski češki njemački estonski engleski francuski talijanski nizozemski portugalski slovački švedski islandski Norwegian
Opis paketa:
- Dostupan samo u poljski
Dodatne informacije
Vrsta prava:
-
Marketing Authorisation
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
- Biowet Pulawy Sp. z o.o.
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
- Biowet Pulawy Sp. z o.o.
Nadležno tijelo:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Broj odobrenja:
- 3218
Datum promjene statusa odobrenja:
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.
poljski (PDF)
Objavljeno na: 7/06/2023
Uputa o lijeku
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
poljski (PDF)
Objavljeno na: 7/06/2023
Označivanje
Ovaj dokument ne postoji na ovom jeziku (hrvatski). U nastavku ga možete pronaći na drugom jeziku.
poljski (PDF)
Objavljeno na: 7/06/2023
