Pulvex Spot (Exspot) 715 mg/mL spot-on solution for dogs
  
        Pulvex Spot (Exspot) 715 mg/mL spot-on solution for dogs
  
Authorised
- Permethrin
Product identification
           Medicine name:        
                    Pulvex Spot (Exspot) 715 mg/mL spot-on solution for dogs
  
                          Exspot 715 mg/ml Lösung zum Auftropfen für Hunde
  
              
          Active substance:        
            - Permethrin
           Target species:        
            - 
Dog
           Route of administration:        
            - 
Spot-on use
Product details
          Active substance and strength:        
            - 
      Permethrin715.00/milligram(s)1.00millilitre(s)
          Pharmaceutical form:        
            - 
Spot-on solution
          Withdrawal period by route of administration:        
            - 
Spot-on use- 
          
Dog
 
- 
          
          Anatomical therapeutic chemical veterinary (ATCvet) codes:        
            - QP53AC04
           Legal status of supply:        
            - 
Veterinary medicinal product subject to veterinary prescription
           Authorisation status:        
            - 
Valid
           Authorised in:        
            - 
Austria
           Available in:        
            - 
Austria
          Package description:        
            - Available only in German
Additional information
          Entitlement type:        
            - 
Marketing Authorisation
          Legal basis of product authorisation:        
            - 
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
           Marketing authorisation holder:        
            - Intervet Ges.m.b.H.
          Marketing authorisation date:        
            
          Manufacturing sites for batch release:        
            - Intervet Productions S.A.
          Responsible authority:        
            - Austrian Agency For Health And Food Safety
          Authorisation number:        
            - 8-00868
          Date of authorisation status change:        
            
          Reference member state:        
            - 
Netherlands
          Procedure number:        
            - NL/V/0137/001
          Concerned member states:        
            - 
Austria
- 
Luxembourg
- 
Slovenia
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
                  This document does not exist in this language (English). You can find it
          in another language below.
              
German (PDF)
 Published on: 20/05/2025
Summary of Product Characteristics
                  This document does not exist in this language (English). You can find it
          in another language below.
              
German (PDF)
 Published on: 20/05/2025
Labelling
                  This document does not exist in this language (English). You can find it
          in another language below.
              
German (PDF)
 Published on: 20/05/2025
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