Xylazine 500 mg 100%, poeder voor oplossing voor parenteraal gebruik
Xylazine 500 mg 100%, poeder voor oplossing voor parenteraal gebruik
Not authorised
- Xylazine hydrochloride
Product identification
Medicine name:
Xylazine 500 mg 100%, poeder voor oplossing voor parenteraal gebruik
Active substance:
- Xylazine hydrochloride
Target species:
-
Zoo animals
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Xylazine hydrochloride50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Powder for solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM92
Legal status of supply:
-
Medicinal product subject to medical prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Netherlands
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 7695
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 24/02/2022