Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Atļautas
- Pentobarbital sodium
Zāļu identifikācija
Zāļu nosaukums:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Aktīvā viela:
- Pieejamas tikai English
Mērķsugas:
-
Liellops
-
Zirgs
-
Cūka
-
Suns
-
Kaķis
Lietošanas veids:
-
intrakardiālai lietošanai
-
intravenozai lietošanai
-
intraperitoneālai lietošanai
Sīkāka informācija par zālēm
Aktīvā viela un stiprums:
-
Pieejamas tikai English400.00/miligrams(i)1.00mililitrs(i)
Farmaceitiskā forma:
-
Šķīdums injekcijām
Ierobežojumu periods pēc lietošanas veida:
-
intrakardiālai lietošanai
-
Liellops
-
Visi attiecīgie audino 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.
-
-
Zirgs
-
Visi attiecīgie audino 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.
-
-
Cūka
-
Visi attiecīgie audino 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.
-
-
-
intravenozai lietošanai
-
Liellops
-
Visi attiecīgie audino 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.
-
-
Zirgs
-
Visi attiecīgie audino 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.
-
-
Cūka
-
Visi attiecīgie audino 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.
-
-
-
intraperitoneālai lietošanai
-
Liellops
-
Visi attiecīgie audino 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.
-
-
Zirgs
-
Visi attiecīgie audino 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.
-
-
Cūka
-
Visi attiecīgie audino 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.
-
-
Anatomiski terapeitiski ķīmiskais veterinārais (ATĶvet) kods:
- QN51AA01
Izplatīšanas juridiskie nosacījumi:
-
Recepšu veterinārās zāles
Atļaujas statuss:
-
Derīga
Iepakojuma apraksts:
- Pieejamas tikai Polish
Papildu informācija
Tiesību tips:
-
Marketing Authorisation
Veterināro zāļu atļaujas piešķiršanas juridiskais pamats:
-
Pieteikums ģenēriskām veterinārajām zālēm (Direktīvas 2001/82/EC 13.(1) pants)
Tirdzniecības atļaujas turētājs:
- Biowet Pulawy Sp. z o.o.
Tirdzniecības atļaujas datums:
Ražošanas vietas sēriju izlaidei:
- Biowet Pulawy Sp. z o.o.
Atbildīgā iestāde:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Atļaujas numurs:
- 3218
Atļaujas statusa maiņas datums:
Lai uzzinātu par veterināro zāļu blakusparādībām, lūdzu, dodieties uz: www.adrreports.eu/vet
Dokumenti
Zāļu apraksts
Šis dokuments neeksistē šādā valodā(latviešu). Jūs to varat atrast citā valodā zemāk.
Polish (PDF)
Publicēts: 7/06/2023
Lietošanas instrukcija
Šis dokuments neeksistē šādā valodā(latviešu). Jūs to varat atrast citā valodā zemāk.
Polish (PDF)
Publicēts: 7/06/2023
Marķējuma teksts
Šis dokuments neeksistē šādā valodā(latviešu). Jūs to varat atrast citā valodā zemāk.
Polish (PDF)
Publicēts: 7/06/2023
