MOXODEX LA 100 MG/ML SOLUTION FOR INJECTION FOR CATTLE
MOXODEX LA 100 MG/ML SOLUTION FOR INJECTION FOR CATTLE
Authorised
- Moxidectin
Product identification
Medicine name:
MOXODEX LA 100 MG/ML SOLUTION FOR INJECTION FOR CATTLE
Moxodex LA 100 mg/mL Solution Injectable pour bovins
Moxodex LA 100 mg/ml oplossing voor injectie voor runderen
Moxodex LA 100 mg/ml Injektionslösung für Rinder
Active substance:
- Moxidectin
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Moxidectin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal108dayThe withdrawal period is based solely on a single injection at the ear site of injection.
-
Milkno withdrawal periodNo withdrawal period
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Box containing 1 vial of 250 mL size
- Box containing 1 vial of 50 mL size
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 Agency For Medicines And Health Products
Authorisation number:
- BE-V662866
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0452/001
Concerned member states:
-
Belgium
-
Ireland
-
Poland
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Labelling
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Package Leaflet
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