Duphamox LA 150 mg/ml Suspensie voor injectie
Duphamox LA 150 mg/ml Suspensie voor injectie
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Duphamox LA 150 mg/ml Suspensie voor injectie
Duphamox LA 150 mg/ml Suspension injectable
Duphamox LA 150 mg/ml Injektionssuspension
Active substance:
- Amoxicillin trihydrate
Target species:
-
Sheep
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Amoxicillin trihydrate150.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal21day.
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
-
Cattle
-
Milk84hour
-
Meat and offal23day
-
-
Pig
-
Meat and offal21day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Duphamox LA 12 250 ml Vial Suspension for injection
- Duphamox LA 12 100 ml Vial Suspension for injection
- Duphamox LA 250 ml Vial Suspension for injection
- Duphamox LA 100 ml Vial Suspension 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:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Manufacturing Limited
- Norbrook Laboratories Limited
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V151182
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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