VIRBAMEC 10 mg/ml injectable solution for cattle
VIRBAMEC 10 mg/ml injectable solution for cattle
Authorised
- Ivermectin
Product identification
Medicine name:
VIRBAMEC 10 mg/ml injectable solution for cattle
VIRBAMEC SOLUTION INJECTABLE POUR BOVINS
Active substance:
- Ivermectin
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption. Do not use in non lactating dairy cows including pregnant heifers within 60 days of calving.
-
Meat and offal49day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- (ID4): 1 unspecified outer container with 1 Bottle (PolyEthylene) with 500 millilitre(s) (500 millilitre(s))
- (ID3): 1 unspecified outer container with 1 Bottle (PolyEthylene) with 50 millilitre(s) (50 millilitre(s))
- (ID2): 1 unspecified outer container with 1 Bottle (PolyEthylene) with 200 millilitre(s) (200 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Bottle (PolyEthylene) with 1000 millilitre(s) (1000 millilitre(s))
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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Sofarimex-Industria Quimica E Farmaceutica S.A.
- VIRBAC
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/2516622 0/2003
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0104/002
Concerned member states:
-
France
-
Luxembourg
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 18/12/2023
Combined File of all Documents
English (PDF)
Download Published on: 14/06/2024
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