Cyclix Porcine solution for injection (87.5 microgram/ml)
Cyclix Porcine solution for injection (87.5 microgram/ml)
Authorised
- Cloprostenol sodium
Product identification
Medicine name:
Cyclix Porcine solution for injection (87.5 microgram/ml)
Сайкликс за свине инжекционен разтвор (87.5 microgram/ml)
Active substance:
- Cloprostenol sodium
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Cloprostenol sodium92.00microgram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG02AD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- (ID2) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s)
- (ID1) 20 millilitre(s): unspecified outer container with 1 Vial (Glass) with 20 millilitre(s)
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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1786
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0112/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
France
-
Hungary
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
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.
Bulgarian (PDF)
Published on: 6/08/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 6/08/2023
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