Animec Super Solution for Injection for Cattle
Animec Super Solution for Injection for Cattle
Authorised
- Clorsulon
- Ivermectin
Product identification
Medicine name:
Animec Super Solution for Injection for Cattle
TOPIMEC SUPER 10 mg/ml / 100 mg/ml injekčný roztok pre hovädzí dobytok
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 permitida a administração a vacas lactantes produtoras de leite destinado ao consumo humano. Não administrar a vacas leiteiras não lactantes, incluindo novilhas gestantes nos 60 dias anteriores à 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:
-
Slovakia
Package description:
- 500 ml High density polyethylene bottle
- 250 ml High density polyethylene bottle
- 50 ml High density polyethylene bottle
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:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/005/MR/22-S
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0133/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Czechia
-
Estonia
-
France
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 29/07/2025
Slovak (PDF)
Published on: 13/04/2022
