Topimec Plus 10/100 mg/ml Solution for Injection for Cattle
Topimec Plus 10/100 mg/ml Solution for Injection for Cattle
Authorised
- Clorsulon
- Ivermectin
Product identification
Medicine name:
Topimec Plus 10/100 mg/ml Solution for Injection for Cattle
Alfamec Fluke 10/100 mg/ml Injektionslösung für Rinder
Livimectim Plus 10/100 mg/ml, soluzione iniettabile per bovini
Active substance:
- Clorsulon
- Ivermectin
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clorsulon100.00/milligram(s)1.00millilitre(s)
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal66dayNão é autorizada a administração a animais produtores de leite para consumo humano. Não administrar a fêmeas gestantes cujo leite é destinado ao consumo humano no prazo de 60 dias antes da data prevista para o parto.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- One HDPE bottle in a cardboard box. 50 ml.
- One HDPE bottle in a cardboard box. 250 ml.
- One HDPE bottle in a cardboard box. 500 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:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401564.00.00
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0137/001
Concerned member states:
-
Belgium
-
France
-
Germany
-
Italy
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
