T 61, injekcinis tirpalas
T 61, injekcinis tirpalas
Authorised
- Embutramide
- Mebezonium iodide
- Tetracaine hydrochloride
Product identification
Medicine name:
T 61, injekcinis tirpalas
Active substance:
- Embutramide
- Mebezonium iodide
- Tetracaine hydrochloride
Target species:
-
Dog
-
Large animals
-
Cat
-
Birds
Route of administration:
-
Intravenous use
-
Intrapulmonary use
Product details
Active substance and strength:
-
Embutramide200.00/milligram(s)1.00millilitre(s)
-
Mebezonium iodide50.00/milligram(s)1.00millilitre(s)
-
Tetracaine hydrochloride5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Dog
-
All relevant tissuesno withdrawal periodT 61 euthanized animals must be disposed of in accordance with national requirements.
-
-
Large animals
-
All relevant tissuesno withdrawal periodDo not use in animals intended for human consumption. T 61 euthanized animals must be disposed of in accordance with national requirements.
-
-
-
Intrapulmonary use
-
Dog
-
All relevant tissuesno withdrawal periodT 61 euthanized animals must be disposed of in accordance with national requirements.
-
-
Cat
-
All relevant tissuesno withdrawal periodT 61 euthanized animals must be disposed of in accordance with national requirements.
-
-
Birds
-
All relevant tissuesno withdrawal periodDo not use in animals intended for human consumption. T 61 euthanized animals must be disposed of in accordance with national requirements.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN51AX50
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/02/1399/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV1399.pdf
Lithuanian (PDF)
Download Published on: 30/06/2022
