PRONILEN 7,5 mg/ml ενέσιμο διάλυμα για άλογα, βοοειδή και πρόβατα
PRONILEN 7,5 mg/ml ενέσιμο διάλυμα για άλογα, βοοειδή και πρόβατα
Authorised
- Luprostiol
Product identification
Medicine name:
PRONILEN 7,5 mg/ml ενέσιμο διάλυμα για άλογα, βοοειδή και πρόβατα
Active substance:
- Luprostiol
Target species:
-
Cattle
-
Horse (mare)
-
Sheep (ewe)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Luprostiol7.50/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal1dayΑγελάδες, μοσχίδες
-
-
Horse (mare)
-
Meat and offalno withdrawal periodΝΑ ΜΗ ΧΟΡΗΓΕΙΤΑΙ ΣΕ ΦΟΡΑΔΕΣ ΠΟΥ ΠΡΟΟΡΙΖΟΝΤΑΙ ΓΙΑ ΑΝΘΡΩΠΙΝΗ ΚΑΤΑΝΑΛΩΣΗ, ΟΥΤΕ ΠΟΥ ΠΑΡΑΓΟΥΝ ΓΑΛΑ ΓΙΑ ΑΝΘΡΩΠΙΝΗ ΚΑΤΑΝΑΛΩΣΗ
-
-
Sheep (ewe)
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG02AD91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
- Intervet International GmbH
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 67284/21-09-2012/K-0044501
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
