VETEGLAN 0.075 mg/ml Solution for injection for cows, sows and mares
VETEGLAN 0.075 mg/ml Solution for injection for cows, sows and mares
Authorised
- Cloprostenol sodium
Product identification
Medicine name:
VETEGLAN 0.075 mg/ml Solution for injection for cows, sows and mares
VETEGLAN 0.075 mg/ml инжекционен разтвор за крави, свине и кобили
Active substance:
- Cloprostenol sodium
Target species:
-
Cattle (cow)
-
Pig
-
Horse (mare)
Route of administration:
-
Solution for injection
Product details
Active substance and strength:
-
Cloprostenol sodium0.08milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Solution for injection
- Cattle (cow)
-
Meat and offal0day
-
Milk0hour
-
- Pig
-
Meat and offal1day
-
- Horse (mare)
-
Meat and offal2day
-
Milk0hour
-
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:
- 20 ml amber coloured Type I glass vials, with Teflon-coated chlorobutyl rubber closures and aluminium seals with blue coloured plastic flip-offs, packaged singly in a cardboard box.
- 10 ml amber coloured Type I glass vials, with Teflon-coated chlorobutyl rubber closures and aluminium seals with blue coloured plastic flip-offs, packaged singly in a cardboard 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:
- Laboratorios Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Calier S.A.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2706
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/100/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Denmark
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Latvia
-
Lithuania
-
Netherlands
-
Romania
-
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: 24/02/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 24/02/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 24/02/2023
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