Virbamec 1% 10 mg/ml Solution injectable
Virbamec 1% 10 mg/ml Solution injectable
Authorised
- Ivermectin
Product identification
Medicine name:
Virbamec 1% 10 mg/ml Solution injectable
Virbamec 1% 10 mg/ml Oplossing voor injectie
Virbamec 1% 10 mg/ml Injektionslösung
Active substance:
- Ivermectin
Target species:
-
Sheep
-
Pig
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Meat and offal45day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
Milkno withdrawal periodDo not use in sheep which are intended to produce milk for human consumption within 60 days of lambing
-
-
Pig
-
Meat and offal35day
-
-
Cattle
-
Meat and offal49day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
Milkno withdrawal periodDo not use in non-lactating dairy cows, including pregnant dairy heifers, within 60 days of calving
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Virbamec 1% 10 mg/ml Solution for injection Vial of 1 l
- Virbamec 1% 10 mg/ml Solution for injection Vial of 500 ml
- Virbamec 1% 10 mg/ml Solution for injection Vial of 200 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
- Sofarimex-Industria Quimica E Farmaceutica S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V277216
Date of authorisation status change:
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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