Zylexis lyofilizát a riedidlo na injekčnú suspenziu pre psov, mačky, kone, hovädzí dobytok a ošípané
Zylexis lyofilizát a riedidlo na injekčnú suspenziu pre psov, mačky, kone, hovädzí dobytok a ošípané
Authorised
- Orf virus, strain D1701, Inactivated
Product identification
Medicine name:
Zylexis lyofilizát a riedidlo na injekčnú suspenziu pre psov, mačky, kone, hovädzí dobytok a ošípané
Active substance:
- Orf virus, strain D1701, Inactivated
Target species:
-
Dog
-
Cat
-
Cattle
-
Horse
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Orf virus, strain D1701, Inactivated1.00relative potency1.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Dog
-
Cat
-
-
Intramuscular use
-
Cattle
-
All relevant tissues0day
-
-
Horse
-
All relevant tissues0day
-
-
Pig
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QL03AX
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
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:
- Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium SA
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/021/05-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 8/07/2024
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