Ceftiomax 50 mg/ml suspension for injection for swine and cattle
Ceftiomax 50 mg/ml suspension for injection for swine and cattle
Authorised
- Ceftiofur
Product identification
Medicine name:
Ceftiomax 50 mg/ml suspension for injection for swine and cattle
Active substance:
- Ceftiofur
Target species:
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Ceftiofur50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal5day
-
-
-
Subcutaneous use
-
Cattle
-
Milk0day
-
Meat and offal8day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Clear glass vial type I of 250 ml with a bromobuthyl pink rubber stopper and aluminium cap gold colour. One vial of 250ml is available in a cardboard box.
- Clear glass vial type I of 100 ml with a bromobuthyl rubber stopper and aluminium cap with opening ring FLIPP OFF of blue colour. One vial of 100ml is available in a cardboard box.
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 Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Calier S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V367035
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0101/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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