Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Authorised
- Pentobarbital sodium
Product identification
Medicine name:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Active substance:
- Pentobarbital sodium
Target species:
-
Cattle
-
Horse
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intracardiac use
-
Intravenous use
-
Intraperitoneal use
Product details
Active substance and strength:
-
Pentobarbital sodium400.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intracardiac use
-
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.
-
-
-
Intravenous use
-
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.
-
-
-
Intraperitoneal use
-
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.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN51AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- Available only in Polish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biowet Pulawy Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Biowet Pulawy Sp. z o.o.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 3218
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 7/06/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 7/06/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 7/06/2023
