MOXAPULVIS 500 mg/g powder for use in drinking water
MOXAPULVIS 500 mg/g powder for use in drinking water
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
MOXAPULVIS 500 mg/g powder for use in drinking water
Active substance:
- Amoxicillin trihydrate
Target species:
-
Turkey
-
Chicken
-
Duck
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate574.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal5day
-
-
Chicken
-
Meat and offal1day
-
-
Duck
-
Meat and offal9day
-
-
Pig
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Round, white HDPE jars that are closed by a polypropylene lid with acardboard/aluminium/PE inner-layer.Pack size: 100 g jar
- Multi-layer laminated bag (Polyester/aluminium foil/polyethylene).Pack size: 1 kg bag
- Round, white HDPE jars that are closed by a polypropylene lid with acardboard/aluminium/PE inner-layer.Pack size: 1 kg jar
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- V.M.D.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0541/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Estonia
-
France
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 27/07/2025