Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Registruotas
- Pentobarbital sodium
Vaisto identifikaciniai duomenys
Vaisto pavadinimas:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Veiklioji medžiaga:
- Pateikiama tik Anglų
Paskirties gyvūnų rūšis (-ys):
-
Galvijai
-
Žirgas
-
Kiaulė
-
Šuo
-
Katė
Naudojimo būdas:
-
Leisti į širdį
-
Leisti į veną
-
Leisti į pilvaplėvės ertmę
Vaisto duomenys
Veiklioji medžiaga ir stiprumas:
-
Pateikiama tik Anglų400.00/miligramai1.00mililitrai
Vaisto forma:
-
Injekcinis tirpalas
Pasitraukimo laikotarpis administravimo būdu:
-
Leisti į širdį
-
Galvijai
-
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.
-
-
Žirgas
-
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.
-
-
Kiaulė
-
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.
-
-
-
Leisti į veną
-
Galvijai
-
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.
-
-
Žirgas
-
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.
-
-
Kiaulė
-
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.
-
-
-
Leisti į pilvaplėvės ertmę
-
Galvijai
-
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.
-
-
Žirgas
-
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.
-
-
Kiaulė
-
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.
-
-
Anatominės, terapinės ir cheminės veterinarinių vaistų klasifikacijos (ATCvet) kodas:
- QN51AA01
Tiekimo teisinis statusas:
-
Parduodama tik su veterinariniu receptu
Registracijos statusas:
-
Valid
Pakuotės aprašymas:
- Pateikiama tik Lenkų
Papildoma informacija
Registruotojas:
- Biowet Pulawy Sp. z o.o.
Rinkodaros leidimo data:
Serijos išleidimo gamybos vietos:
- Biowet Pulawy Sp. z o.o.
Atsakinga institucija:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Registracijos numeris:
- 3218
Registracijos statuso pasikeitimo data:
Pranešimai apie įtariamus nepageidaujamus reiškinius: www.adrreports.eu/vet
Dokumentai
Veterinarinio vaisto aprašas
Šis dokumentas neegzistuoja šia kalba (Lietuvių). Jį galite rasti kita kalba žemiau.
Lenkų (PDF)
Paskelbta: 7/06/2023
Pakuotės lapelis
Šis dokumentas neegzistuoja šia kalba (Lietuvių). Jį galite rasti kita kalba žemiau.
Lenkų (PDF)
Paskelbta: 7/06/2023
Ženklinimas
Šis dokumentas neegzistuoja šia kalba (Lietuvių). Jį galite rasti kita kalba žemiau.
Lenkų (PDF)
Paskelbta: 7/06/2023