Oxytocine Kela 10 IU/ml Oplossing voor injectie
Oxytocine Kela 10 IU/ml Oplossing voor injectie
Authorised
- Oxytocin
Product identification
Medicine name:
Oxytocine Kela 10 IU/ml Oplossing voor injectie
Oxytocine Kela 10 IU/ml Solution injectable
Oxytocine Kela 10 IU/ml Injektionslösung
Active substance:
- Oxytocin
Target species:
-
Sheep
-
Goat
-
Dog
-
Cat
-
Pig
-
Cattle
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Oxytocin10.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Dog
-
Cat
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Horse
-
Milk0day
-
Meat and offal0day
-
-
-
Intravenous use
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Dog
-
Cat
-
-
Subcutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Oxytocine Kela 12 x 100 ml Vial Solution for injection
- Oxytocine Kela 12 x 50 ml Vial Solution for injection
- Oxytocine Kela 12 x 30 ml Vial Solution for injection
- Oxytocine Kela 12 x 10 ml Vial Solution for injection
- Oxytocine Kela 1 x 100 ml Vial Solution for injection
- Oxytocine Kela 1 x 50 ml Vial Solution for injection
- Oxytocine Kela 1 x 30 ml Vial Solution for injection
- Oxytocine Kela 1 x 10 ml Vial Solution for injection
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:
- Kela Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V286072
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
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Package Leaflet
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Labelling
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