KALIPROFEN LA 50 mg/ml raztopina za injiciranje za govedo
KALIPROFEN LA 50 mg/ml raztopina za injiciranje za govedo
Authorised
- Carprofen
Product identification
Medicine name:
KALIPROFEN LA 50 mg/ml raztopina za injiciranje za govedo
Active substance:
- Carprofen
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Carprofen50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal21dayMeso in organi: 21 dni
-
Milk0hourMleko: nič ur
-
-
-
Intravenous use
-
Cattle
-
Milk0hourMleko: nič ur
-
Meat and offal21dayMeso in organi: 21 dni
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- GENERA SI podjetje za zastopanje in trgovino d.o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0418/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 28/11/2021
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 28/11/2021
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