ACTIONIS 50 mg/ml, suspension for injection for pigs and cattle
ACTIONIS 50 mg/ml, suspension for injection for pigs and cattle
Authorised
- Ceftiofur hydrochloride
Product identification
Medicine name:
ACTIONIS 50 mg/ml zawiesina do wstrzykiwań dla świń i bydła
ACTIONIS 50 mg/ml, suspension for injection for pigs and cattle
Active substance:
- Ceftiofur hydrochloride
Target species:
-
Cattle
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Ceftiofur hydrochloride50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal6day
-
Milk0hour
-
-
Cattle
-
Meat and offal6day
-
Milk0hour
-
-
-
Intramuscular use
-
Pig
-
Meat and offal6day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- box containing 1 PET vial of 250 ml
- box containing 1 PET vial of 100 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) 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.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2181
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0157/001
Concerned member states:
-
Germany
-
Hungary
-
Italy
-
Poland
-
Portugal
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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