Veterinary Medicines

Milipraz 12.5 mg/125 mg Chewable Tablets for dogs

Authorised
  • Milbemycin oxime
  • Praziquantel
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Product identification

Medicine name:
MILIPRAZ 12.5 MG/125 MG CHEWABLE TABLETS FOR DOGS
Milipraz 12.5 mg/125 mg Chewable Tablets for dogs
Active substance:
  • Milbemycin oxime
  • Praziquantel
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Milbemycin oxime
    12.50
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    125.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Chewable tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AB51
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Box with 1 blister strip of 4 chewable tablets
  • Box with 2 blister strips of 5 chewable tablets
  • Box with 3 blister strips of 4 chewable tablets
  • Box with 5 blister strips of 4 chewable tablets
  • Box with 6 blister strips of 4 chewable tablets
  • Box with 12 blister strips of 4 chewable tablets
  • box with 1 blister of 2 chewable tablets
  • Box with 2 blister of 2 chewable tablets
  • Box with 1 blister strips of of 5 chewable tablets
  • Box with 5 blisters, each blister of 2 chewable tablets
  • Box with of 6 blister strips of 2 chewable tablets
  • Box with 3 blister strips of 5 chewable tablets
  • Box with 10 blisters strips of 2 chewable tablets
  • Box with 12 blister strips of 2 chewable tablets
  • Box with 5 blister strips of 5 chewable tablets
  • Box with 6 blister strips of 5 chewable tablets
  • Box with 5 blister strips of 10 chewable tablets
  • Box with 8 blister strips of 5 chewable tablets
  • Box with 9 blister strips of 5 chewable tablets
  • Box with 24 blisters strips of 2 chewable tablets
  • Box with 10 blister strips of 5 chewable tablets

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10987/182/001
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0487/001
Concerned member states:
  • Ireland
Generic of:

Documents

eu-puar-frv0487001-mr-rpe943-en.pdf

English (PDF)
Published on: 7/01/2026
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