MILBETAB 4 MG/10 MG FILM-COATED TABLETS FOR SMALL CATS AND KITTENS
MILBETAB 4 MG/10 MG FILM-COATED TABLETS FOR SMALL CATS AND KITTENS
Authorised
- Milbemycin oxime
- Praziquantel
Product identification
Medicine name:
MILBETAB 4 MG/10 MG FILM-COATED TABLETS FOR SMALL CATS AND KITTENS
Milbetab 4 mg/10 mg comprimidos revestidos por película para gatos pequenos e gatinhos
Active substance:
- Milbemycin oxime
- Praziquantel
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Milbemycin oxime4.00/milligram(s)1.00Tablet
-
Praziquantel10.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- Cardboard box with 2 tablets (1 blister strip of 2)
- Cardboard box with 4 tablets (1 blister strip of 4)
- Cardboard box with 10 tablets (1 blister strip of 10)
- Cardboard box with 20 tablets (2 blister strips of 10)
- Cardboard box with 50 tablets (5 blister strips of 10)
- Cardboard box with 100 tablets (10 blister strips of 10)
- Multipacks of 10 individual packs of 2 tablets
- Multipacks of 10 individual packs of 20 tablets
- Multipacks of 10 individual packs of 50 tablets
- Cardboard box with 4 tablets (2 blister strips of 2)
- Cardboard box with 10 tablets (5 blisters strips of 2)
- Cardboard box with 20 tablets (10 blisters strips of 2)
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:
- Directorate General For Food And Veterinary
Authorisation number:
- 1703/02/25DFVPT
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0475/002
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 17/06/2025