DRAXXIN PLUS
DRAXXIN PLUS
Authorised
- Ketoprofen
- Tulathromycin
Product identification
Medicine name:
DRAXXIN PLUS
Draxxin Plus 100 mg/ml + 120 mg/ml oldatos injekció szarvasmarhák számára A.U.V.
Active substance:
- Ketoprofen
- Tulathromycin
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ketoprofen120.00milligram(s)1.00millilitre(s)
-
Tulathromycin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Milkno withdrawal periodNot authorised for use in cattle producing milk for human consumption. Do not use in pregnant animals, which are intended to produce milk for human consumption, within 2 months of expected parturition.
-
Meat and offal50day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01FA99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Available in:
-
Hungary
Package description:
- cardboard box containing 1 vial of 250 ml
- cardboard box containing 1 vial of 100 ml
- cardboard box containing 1 vial of 50 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Fixed combination application (Article 13b of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Hungary Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain, S.L.
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
- 4174/X/20 NÉBIH ÁTI
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0352/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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