Milbemycin oxime Praziquantel Chew Alfamed 25.0 mg / 250.0 mg chewable tablets for large dogs
Milbemycin oxime Praziquantel Chew Alfamed 25.0 mg / 250.0 mg chewable tablets for large dogs
Authorised
- Milbemycin oxime
- Praziquantel
Product identification
Medicine name:
Milbemycin oxime Praziquantel Chew Alfamed 25.0 mg / 250.0 mg chewable tablets for large dogs
Milbemycin oxime Praziquantel Chew Alfamed 25,0 mg / 250,0 mg comprimés à croquer pour grands chiens
Milbemycin oxime Praziquantel Chew Alfamed 25,0 mg / 250,0 mg kauwtablet voor grote honden
Milbemycin oxime Praziquantel Chew Alfamed 25,0 mg / 250 mg Kautabletten für große Hunde
Active substance:
- Milbemycin oxime
- Praziquantel
Target species:
-
Dog (large)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Milbemycin oxime25.00/milligram(s)1.00Tablet
-
Praziquantel25.00/milligram(s)1.00Tablet
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:
-
Belgium
Package description:
- 1 box with 1 blister, each blister contains 2 chewable tablets
- 1 box with 2 blisters, each blister contains 2 chewable tablets
- 1 box with 12 blisters, each blister contains 2 chewable tablets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 19(1) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Alfamed
Marketing authorisation date:
Manufacturing sites for batch release:
- Alfamed
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V663733
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0413/003
Concerned member states:
-
Belgium
-
France
-
Germany
-
Ireland
-
Italy
-
Norway
-
Portugal
-
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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Labelling
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Package Leaflet
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