T 61 Solution injectable
T 61 Solution injectable
Authorised
- Tetracaine hydrochloride
- Embutramide
- Mebezonium iodide
Identification du produit
Dénomination du médicament:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Voie d’administration:
-
Voie intrabronchique
-
Voie intracardiaque
-
Voie intraveineuse
Informations sur le produit
Forme pharmaceutique:
-
Solution injectable
Withdrawal period by route of administration:
-
Intrapulmonary use
- Chien
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
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- Chat
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Vison
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Oiseaux de volière
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Laboratory animals
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Pigeon
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Intracardiac use
- Chien
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Intravenous use
- Bovins
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Cheval
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
- Chien
-
Viande et abatsno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
Code anatomique, thérapeutique, chimique, vétérinaire (ATCvet):
- QN51AX50
Statut juridique de la production:
-
Médicament vétérinaire soumis à prescription vétérinaire
Statut de l’autorisation:
-
Valide
Authorised in:
-
Belgique
Description de l’emballage:
- Disponible uniquement en English
Informations supplémentaires
Entitlement type:
-
Autorisation de mise sur le marché
Titulaire de l’autorisation de mise sur le marché:
- Intervet International B.V.
Marketing authorisation date:
Sites de fabrication pour la libération des lots:
- Intervet International GmbH
Autorité responsable:
- FAMHP
Numéro de l’autorisation:
- BE-V179304
Date de modification du statut de l’autorisation:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Résumé des caractéristiques du produit
français (PDF)
Télécharger Publié le: 22/03/2022
Dutch (PDF)
Publié le: 22/03/2022
Notice
français (PDF)
Télécharger Publié le: 22/03/2022
Dutch (PDF)
Publié le: 22/03/2022
German (PDF)
Publié le: 22/03/2022
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