CLOXALENE PLUS 110 mg/ml + 50 mg/ml ενέσιμο εναιώρημα για άλογα, βοοειδή, χοίρους, σκύλους, γάτες
CLOXALENE PLUS 110 mg/ml + 50 mg/ml ενέσιμο εναιώρημα για άλογα, βοοειδή, χοίρους, σκύλους, γάτες
Authorised
- Ampicillin trihydrate
- Dicloxacillin sodium monohydrate
Product identification
Medicine name:
CLOXALENE PLUS 110 mg/ml + 50 mg/ml ενέσιμο εναιώρημα για άλογα, βοοειδή, χοίρους, σκύλους, γάτες
Active substance:
- Ampicillin trihydrate
- Dicloxacillin sodium monohydrate
Target species:
-
Horse
-
Cattle
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Ampicillin trihydrate11.00/gram(s)100.00millilitre(s)
-
Dicloxacillin sodium monohydrate5.00/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Horse
-
Meat and offal7dayγια το σημείο ενέσεως 28 ημέρες
-
Milk5day
-
- Cattle
-
Meat and offal7dayγια το σημείο ενέσεως 28 ημέρες
-
Milk5day
-
- Pig
-
Meat and offal7dayγια το σημείο ενέσεως 28 ημέρες
-
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR50
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 1103/15-01-1992/K-0042001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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