OXYVET 500mg/τεμάχιο ΠΕΣΣΟΙ
OXYVET 500mg/τεμάχιο ΠΕΣΣΟΙ
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
OXYVET 500mg/τεμάχιο ΠΕΣΣΟΙ
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Goat
-
Cattle (cow)
-
Horse (mare)
-
Sheep (ewe)
-
Pig (sow)
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride500.00/milligram(s)1.00Pessary
Pharmaceutical form:
-
Pessary
Withdrawal period by route of administration:
-
Intrauterine use
-
Goat
-
Meat and offal28day
-
Milk48hour
-
-
Cattle (cow)
-
Meat and offal28day
-
Milk48hour
-
-
Horse (mare)
-
Meat and offal28dayΓΑΛΑ: να μη χορηγείται σε φοράδες των οποίων το γάλα προορίζεται για ανθρώπινη κατανάλωση
-
-
Sheep (ewe)
-
Meat and offal28day
-
Milk48hour
-
-
Pig (sow)
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG01AA07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- PROVET S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- PROVET S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 31820/29-04-2021/K-0005408
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet