Oxytocin aniMedica
Oxytocin aniMedica
Authorised
- Oxytocin
Product identification
Medicine name:
Oxytocin aniMedica
Active substance:
- Oxytocin
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Horse
-
Cat
-
Pig
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
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- 10 ml Vial: colourless glass vial (Type HK1).Stopper : Rubber stopper of grey bromobutyl rubber.Cap : Medium gold flanged cap.Pack size: 10 ml.
- 50 ml Vial: colourless glass vial (Type HK2).Stopper : Rubber stopper of grey bromobutyl rubber.Cap : Medium gold flanged cap.Pack size: 12 x 50 ml.
- 50 ml Vial: colourless glass vial (Type HK2).Stopper : Rubber stopper of grey bromobutyl rubber.Cap : Medium gold flanged cap.Pack size: 50 ml.
- 10 ml Vial: colourless glass vial (Type HK1).Stopper : Rubber stopper of grey bromobutyl rubber.Cap : Medium gold flanged cap.Pack size: 12 x 10 ml.
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:
- aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- aniMedica Herstellungs GmbH
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10826/004/001
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
English (PDF)
Download Published on: 3/05/2024
How useful was this page?: