Veterinary Medicine Information website

Metrobactin 250 mg tablets for cats and dogs

Authorised
  • Metronidazole
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Product identification

Medicine name:
Metrobactin 250 mg tablets for cats and dogs
Active substance:
  • Metronidazole
Target species:
  • Dog
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Metronidazole
    250.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01XD01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 9 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 8 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 6 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 50 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 7 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 3 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 25 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 5 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 4 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 1 blister of 10 tablets.
  • Aluminium - PVC/PE/PVDC blister. Cardboard box containing 10 boxes, each containing 10 blisters of 10 tablets.
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 2 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box of 10 blisters of 10 tablets
  • Aluminium - PVC/PE/PVDC blister. Cardboard box containing 10 boxes, each containing 1 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:
  • Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lelypharma B.V.
  • Genera d.d.
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 104847
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0193/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 7/07/2023
Updated on: 9/07/2023
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