Apravet 552 000 IU/g powder for use in drinking water/milk for pigs, calves, chickens and rabbits
Apravet 552 000 IU/g powder for use in drinking water/milk for pigs, calves, chickens and rabbits
Authorised
- Apramycin sulfate
Product identification
Medicine name:
Apravet 552 000 IU/g powder for use in drinking water/milk for pigs, calves, chickens and rabbits
Active substance:
- Apramycin sulfate
Target species:
-
Pig (weaned piglet)
-
Rabbit
-
Cattle (pre-ruminant)
-
Chicken (broiler)
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Apramycin sulfate1.00/milligram(s)1.00milligram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Pig (weaned piglet)
-
Meat and offal0day
-
-
Rabbit
-
Meat and offal0day
-
-
Cattle (pre-ruminant)
-
Meat and offal28day
-
-
Chicken (broiler)
-
Meat and offal0day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA92
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- box containing 50 sachets of 1,812 g
- box containing 25 sachets of 1,812 g
- bottle containing 90,58 g
- bag containing 1811,6 g
- 1 Sachet with 1,812g
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:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet AD
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:
-
Spain
Procedure number:
- ES/V/0252/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Labelling
This document does not exist in this language (English). You can find it in another language below.
eu-PUAR-esv0252001-dcp-apravet-soluble-powder-en.pdf
English (PDF)
Download Published on: 21/12/2023