Metrotab vet. Flavoured 500 mg Tablets for dogs and cats
  
        Metrotab vet. Flavoured 500 mg Tablets for dogs and cats
  
Authorised
- Metronidazole
 
Product identification
           Medicine name:        
                    Metrotab vet. Flavoured 500 mg Tablets for dogs and cats
  
                          Metrotab vet. Flavoured 500 mg Tabletten für Hunde und Katzen
  
              
          Active substance:        
            - Metronidazole
 
           Target species:        
            - 
Dog
 - 
Cat
 
           Route of administration:        
            - 
Oral use
 
Product details
          Active substance and strength:        
            - 
      Metronidazole500.00/milligram(s)1.00Tablet
 
          Pharmaceutical form:        
            - 
Tablet
 
          Withdrawal period by route of administration:        
            - 
Oral use
- 
          
Dog
 - 
          
Cat
 
 - 
          
 
          Anatomical therapeutic chemical veterinary (ATCvet) codes:        
            - QJ01XD01
 - QP51AA01
 
           Legal status of supply:        
            - 
Veterinary medicinal product subject to veterinary prescription
 
           Authorisation status:        
            - 
Valid
 
           Authorised in:        
            - 
Germany
 
           Available in:        
            - 
Germany
 
          Package description:        
            - Aluminium - PVC/PE/PVDC cardboard box with 10 blisters of 10 tablets.
 - Aluminium - PVC/PE/PVDC cardboard box with 5 blisters of 10 tablets.
 - Aluminium - PVC/PE/PVDC cardboard box with 3 blisters of 10 tablets.
 - Aluminium - PVC/PE/PVDC cardboard box with 2 blisters of 10 tablets.
 
Additional information
          Entitlement type:        
            - 
Marketing Authorisation
 
          Legal basis of product authorisation:        
            - 
Generic application (Article 13(1) of Directive No 2001/82/EC)
 
           Marketing authorisation holder:        
            - CP-Pharma Handelsgesellschaft mbH
 
          Marketing authorisation date:        
            
          Manufacturing sites for batch release:        
            - CP-Pharma Handelsgesellschaft mbH
 
          Responsible authority:        
            - Federal Office Of Consumer Protection And Food Safety
 
          Authorisation number:        
            - 402760.00.00
 
          Date of authorisation status change:        
            
          Reference member state:        
            - 
Netherlands
 
          Procedure number:        
            - NL/V/0350/002
 
          Concerned member states:        
            - 
Austria
 - 
Belgium
 - 
Denmark
 - 
Finland
 - 
France
 - 
Germany
 - 
Hungary
 - 
Ireland
 - 
Italy
 - 
Poland
 - 
Portugal
 - 
Spain
 - 
Sweden
 - 
United Kingdom (Northern Ireland)
 
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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