MILBEMAX 2.5 MG/25 MG CHEWABLE TABLETS FOR SMALL DOGS AND PUPPIES
MILBEMAX 2.5 MG/25 MG CHEWABLE TABLETS FOR SMALL DOGS AND PUPPIES
Authorised
- Milbemycin oxime
- Praziquantel
Product identification
Medicine name:
MILBEMAX 2.5 MG/25 MG CHEWABLE TABLETS FOR SMALL DOGS AND PUPPIES
Milbemax voor kleine honden en puppys 2.5 mg - 25 mg Kauwtablet
Milbemax voor kleine honden en puppys 2.5 mg - 25 mg Comprimé à croquer
Milbemax voor kleine honden en puppys 2.5 mg - 25 mg Kautablette
Active substance:
- Milbemycin oxime
- Praziquantel
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Milbemycin oxime2.50milligram(s)1.00Tablet
-
Praziquantel25.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Chewable tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- 1 box with 1 blister of 2 chewable tablets
- 1 box with 12 strips, each strip contains 4 chewable tablets
- 1 box with 12 blisters, each blister contains 4 chewable tablets
- 1 box with 1 strip of 4 chewable tablets
- 1 box with 1 strip of 2 chewable tablets
- 1 box with 1 blister of 4 chewable tablets
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:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Elanco France S.A.S.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0135/005
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Labelling
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