Ivomec 1% 10 mg/ml Oplossing voor injectie
Ivomec 1% 10 mg/ml Oplossing voor injectie
Authorised
- Ivermectin
Product identification
Medicine name:
Ivomec 1% 10 mg/ml Oplossing voor injectie
Ivomec 1% 10 mg/ml Solution injectable
Ivomec 1% 10 mg/ml Injektionslösung
Active substance:
- Ivermectin
Target species:
-
Sheep
-
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 offal22dayNiet gebruiken bij melkooien buiten lactatie binnen 60 dagen voor de partus. Ne pas utiliser chez les brebis laitières hors lactation dans les 60 jours précédant la mise bas.
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Cattle
-
Meat and offal49dayNiet gebruiken bij melkkoeien in droogstand, met inbegrip van drachtige melkvaarzen binnen 60 dagen voor de partus. Ne pas utiliser chez les vaches laitières en période de tarissement, y compris les génisses laitières gestantes dans les 60 jours précédant la mise bas.
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-
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:
- Ivomec 1% 1 l Vial Solution for injection
- Ivomec 1% 500 ml Vial Solution for injection
- Ivomec 1% 200 ml Vial Solution for injection
- Ivomec 1% 50 ml Vial Solution for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France SCS
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V120556
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Labelling
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