Oxytocina Pituitaria Calier 20 IU/ml šķīdums injekcijām liellopiem, zirgiem, aitām, kazām, cūkām, suņiem un kaķiem
Oxytocina Pituitaria Calier 20 IU/ml šķīdums injekcijām liellopiem, zirgiem, aitām, kazām, cūkām, suņiem un kaķiem
Not authorised
- Oxytocin
Product identification
Medicine name:
Oxytocina Pituitaria Calier 20 IU/ml šķīdums injekcijām liellopiem, zirgiem, aitām, kazām, cūkām, suņiem un kaķiem
Active substance:
- Oxytocin
Target species:
-
Pig
-
Dog
-
Cat
-
Goat
-
Horse
-
Cattle
-
Sheep
Route of administration:
-
Intravenous use
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Oxytocin20.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Pig
-
Meat and offal2day
-
-
Goat
-
Milk2day
-
Meat and offal2day
-
-
Horse
-
Milk2day
-
Meat and offal2day
-
-
Cattle
-
Milk2day
-
Meat and offal2day
-
-
Sheep
-
Milk2day
-
Meat and offal2day
-
-
-
Intramuscular use
-
Pig
-
Meat and offal2day
-
-
Sheep
-
Milk2day
-
Meat and offal2day
-
-
Cattle
-
Milk2day
-
Meat and offal2day
-
-
Horse
-
Meat and offal2day
-
Milk2day
-
-
Goat
-
Meat and offal2day
-
Milk2day
-
-
-
Subcutaneous use
-
Pig
-
Meat and offal2day
-
-
Cattle
-
Meat and offal2day
-
Milk2day
-
-
Horse
-
Meat and offal2day
-
Milk2day
-
-
Sheep
-
Meat and offal2day
-
Milk2day
-
-
Goat
-
Meat and offal2day
-
Milk2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Latvia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Laboratorios Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Calier S.A.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/01/1291
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
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 9/06/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 9/06/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 9/06/2025