FACILPART, 10 TV/ml injekcinis tirpalas
FACILPART, 10 TV/ml injekcinis tirpalas
Authorised
- Oxytocin
Product identification
Medicine name:
FACILPART, 10 TV/ml injekcinis tirpalas
Active substance:
- Oxytocin
Target species:
-
Cattle (cow)
-
Horse (mare)
-
Pig (female)
-
Sheep (ewe)
-
Goat (adult female)
-
Dog (bitch)
-
Cat (adult female)
Route of administration:
-
Intravenous use
-
Intramuscular 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:
-
Intravenous use
- Cattle (cow)
-
Meat and offal, milk0day
-
- Horse (mare)
-
Meat and offal, milk0day
-
- Pig (female)
-
Meat and offal0day
-
- Sheep (ewe)
-
Meat and offal, milk0day
-
- Goat (adult female)
-
Meat and offal, milk0day
-
- Dog (bitch)
- Cat (adult female)
-
Intramuscular use
- Cattle (cow)
-
Meat and offal, milk0day
-
- Horse (mare)
-
Meat and offal, milk0day
-
- Pig (female)
-
Meat and offal0day
-
- Sheep (ewe)
-
Meat and offal, milk0day
-
- Goat (adult female)
-
Meat and offal, milk0day
-
- Dog (bitch)
- Cat (adult female)
-
Subcutaneous use
- Cattle (cow)
-
Meat and offal, milk0day
-
- Horse (mare)
-
Meat and offal, milk0day
-
- Pig (female)
-
Meat and offal0day
-
- Sheep (ewe)
-
Meat and offal, milk0day
-
- Goat (adult female)
-
Meat and offal, milk0day
-
- Dog (bitch)
- Cat (adult female)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
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:
- Laboratorios Syva S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Syva S.A.U.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/11/2063/001-005
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV2063.pdf
Lithuanian (PDF)
Download Published on: 1/03/2024
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