FUREXEL COMBI ORAL PASTE
FUREXEL COMBI ORAL PASTE
Authorised
- Ivermectin
- Praziquantel
Product identification
Medicine name:
FUREXEL COMBI ORAL PASTE
Furexel Combi Pasta voor oraal gebruik
Furexel Combi P�te orale
Furexel Combi Paste zum Einnehmen
Active substance:
- Ivermectin
- Praziquantel
Target species:
-
Horse
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Ivermectin15.50gram(s)1.00gram(s)
-
Praziquantel77.50gram(s)1.00gram(s)
Pharmaceutical form:
-
Oral paste
Withdrawal period by route of administration:
-
Oral use
-
Horse
-
Meat and offal30day
-
Milkno withdrawal periodDo not use in mares producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France SCS
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V279221
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0360/001
Concerned member states:
-
Belgium
-
Germany
-
Luxembourg
-
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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