PARTOVET
PARTOVET
Authorised
- Oxytocin
Product identification
Medicine name:
PARTOVET
Active substance:
- Oxytocin
Target species:
-
Horse (mare)
-
Dog (bitch)
-
Cat (adult female)
-
Goat (adult female)
-
Cattle (cow)
-
Pig (female)
-
Sheep (ewe)
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
-
Horse (mare)
-
Meat and offal0day
-
Milk0day
-
-
Dog (bitch)
-
Cat (adult female)
-
Goat (adult female)
-
Meat and offal0day
-
Milk0day
-
-
Cattle (cow)
-
Meat and offal0day
-
Milk0day
-
-
Pig (female)
-
Meat and offal0day
-
-
Sheep (ewe)
-
Meat and offal0day
-
Milk0day
-
-
-
Intravenous use
-
Horse (mare)
-
Meat and offal0day
-
Milk0day
-
-
Dog (bitch)
-
Cat (adult female)
-
Goat (adult female)
-
Meat and offal0day
-
Milk0day
-
-
Cattle (cow)
-
Meat and offal0day
-
Milk0day
-
-
Pig (female)
-
Meat and offal0day
-
-
Sheep (ewe)
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Horse (mare)
-
Meat and offal0day
-
Milk0day
-
-
Dog (bitch)
-
Cat (adult female)
-
Goat (adult female)
-
Meat and offal0day
-
Milk0day
-
-
Cattle (cow)
-
Meat and offal0day
-
Milk0day
-
-
Pig (female)
-
Meat and offal0day
-
-
Sheep (ewe)
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Divasa Farmavic S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- DIVASA-FARMAVIC, S.A.
Responsible authority:
- Spanish Agency For Medicines And Health Products
Authorisation number:
- 449 ESP
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.
Spanish (PDF)
Published on: 8/11/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 8/11/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 8/11/2022
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