MILPRO 16 MG/40 MG FILM-COATED TABLETS FOR CATS
MILPRO 16 MG/40 MG FILM-COATED TABLETS FOR CATS
Authorised
- Milbemycin oxime
- Praziquantel
Product identification
Medicine name:
MILPRO 16 MG/40 MG FILM-COATED TABLETS FOR CATS
Milpro 16 mg/40 mg, plėvele dengtos tabletės katėms
Active substance:
- Milbemycin oxime
- Praziquantel
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Milbemycin oxime16.00milligram(s)1.00Tablet
-
Praziquantel40.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Withdrawal period by route of administration:
-
Oral use
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Available in:
-
Lithuania
Package description:
- Cardboard box of 2 tablets containing 1 blister of 2 tablets (divisible per tablet)
- Cardboard box of 48 tablets containing 24 blisters of 2 tablets (divisible per tablet)
- Cardboard box of 24 tablets containing 12 blisters of 2 tablets (divisible per tablet)
- Cardboard box of 4 tablets containing 2 blisters of 2 tablets (divisible per tablet)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/14/2225/001-004
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0390/004
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV2225.pdf
Lithuanian (PDF)
Download Published on: 15/01/2025
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