Ovarelin 50 ug/ml, solution for injection for cattle
Ovarelin 50 ug/ml, solution for injection for cattle
Authorised
- GONADORELIN DIACETATE TETRAHYDRATE
Product identification
Medicine name:
Ovarelin 50 ug/ml, solution for injection for cattle
Ovarelin 50 µg/ml Oplossing voor injectie
Ovarelin 50 µg/ml Solution injectable
Ovarelin 50 µg/ml Injektionslösung
Active substance:
- GONADORELIN DIACETATE TETRAHYDRATE
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
GONADORELIN DIACETATE TETRAHYDRATE58.13/microgram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Material of the primary container:Colourless glass vial type I (4 ml).Chlorobutyl stopper.Pack size:Box containing 1 glass vial of 4 ml
- Material of the primary container:Colourless glass vial type II (10 ml).Chlorobutyl stopper.Pack size:Box containing 1 glass vial of 10 ml
- Material of the primary container:Colourless glass vial type II (20 ml).Chlorobutyl stopper.Pack size:Box containing 1 glass vial of 20 ml
- Material of the primary container:Colourless glass vial type II (50 ml).Chlorobutyl stopper.Pack size:Box containing 1 glass vial of 50 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- CEVA SANTE ANIMALE
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0598/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Hungary
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Sweden
-
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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