Varroxal 0,71 g/g bee-hive powder
Varroxal 0,71 g/g bee-hive powder
Authorised
This information is not available for this product.
Product identification
Medicine name:
Varroxal 0,71 g/g bee-hive powder
Varroxal 0,71 g/g prašek za čebeljo družino
Active substance:
This information is not available for this product.
Target species:
-
Honey bee
Route of administration:
-
Topical use
Product details
Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
-
Powder
Withdrawal period by route of administration:
-
Topical use
- Honey bee
-
Honeyno withdrawal periodNul dagen
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AG03
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Package description:
- Cardboard box with a 200 g HDPE bottle closed with an ALU/HDPE seal and a HDPE/ PP turn and lock cap and 1 g measuring spoon
- Cardboard box with a 75 g HDPE bottle closed with an ALU/HDPE seal and a HDPE/ PP turn and lock cap and 1 g measuring spoon
- Cardboard box with a PET/ALU/PE bag containing 50 x 2g sealed paper-PE sachets.
- Cardboard box with a PET/ALU/PE bag containing 10 x 2g sealed paper-PE sachets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Andermatt BioVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Andermatt Biovet GmbH
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- MR/V/0789/001
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0402/001
Concerned member states:
-
Austria
-
Croatia
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 8/04/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 8/04/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 8/04/2024
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