Milprazon 16 mg/40 mg film-coated tablets for cats weighing at least 2 kg
Milprazon 16 mg/40 mg film-coated tablets for cats weighing at least 2 kg
Authorised
- Milbemycin oxime
- Praziquantel
Product identification
Medicine name:
Milprazon 16 mg/40 mg film-coated tablets for cats weighing at least 2 kg
Milprazon 16 mg/40 mg Filmtabletten für Katzen mit einem Gewicht von mindestens 2 kg
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:
-
Germany
Package description:
- Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 1 blister of 2 tablets.
- Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 1 blister of 4 tablets.
- Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 12 blisters, each blister contains 4 tablets.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
- TAD Pharma GmbH
- Krka-Farma d.o.o.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402099.00.00
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0464/002
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
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
Summary of Product Characteristics
English (PDF)
Download Published on: 26/08/2024
Updated on: 18/12/2024
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 18/12/2024
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