Rycarfa 50 mg/ml solution for injection for dogs and cats
Rycarfa 50 mg/ml solution for injection for dogs and cats
Authorised
- Carprofen
Product identification
Medicine name:
Rycarfa 50 mg/ml solution for injection for dogs and cats
Rycarfa 50 mg/ml Oplossing voor injectie
Rycarfa 50 mg/ml Solution injectable
Rycarfa 50 mg/ml Injektionslösung
Active substance:
- Carprofen
Target species:
-
Dog
-
Cat
Route of administration:
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Carprofen50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Dog
-
Cat
-
-
Subcutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Type I glass vial (amber glass): 1 vial of 20 ml solution for injection with bromobutyl rubber stopper and aluminium seal, in a box.
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
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V456995
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0317/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Italy
-
Netherlands
-
Norway
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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