XYLAZIN Ecuphar, 20mg/ml, Injekční roztok
XYLAZIN Ecuphar, 20mg/ml, Injekční roztok
Authorised
- Xylazine hydrochloride
Product identification
Medicine name:
XYLAZIN Ecuphar, 20mg/ml, Injekční roztok
Active substance:
- Xylazine hydrochloride
Target species:
-
Horse
-
Cattle
-
Dog
-
Cat
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Xylazine hydrochloride23.30/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Horse
-
Meat and offal1day
-
Milk0hour
-
-
Cattle
-
Meat and offal1day
-
Milk0hour
-
-
-
Intramuscular use
-
Cattle
-
Meat and offal1day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM92
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Available in:
-
Czechia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ecuphar
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta, a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/006/02-C
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.
Czech (PDF)
Published on: 11/05/2023
Package Leaflet
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in another language below.
Czech (PDF)
Published on: 11/05/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 11/05/2023