Parofor 70000 IU/g Powder for use in drinking water/milk
Parofor 70000 IU/g Powder for use in drinking water/milk
Authorised
- Paromomycin
Product identification
Medicine name:
Parofor 70000 IU/g Powder for use in drinking water/milk
Parofor 70000 IU/g Poeder voor toediening in het drinkwater/in de melk
Parofor 70000 IU/g Poudre pour administration dans le lait ou l'eau de boisson
Parofor 70000 IU/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
- Paromomycin
Target species:
-
Cattle
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Paromomycin70000.00/international unit(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle
-
Meat and offal20day20 days for pre-ruminant cattle
-
-
Pig
-
Meat and offal3day3 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- 1000g: sachet (PE/ALU/PET) with 1000g powder
- 500g: sachet (PE/ALU/PET) with 500g powder
- 250g: sachet (PE/ALU/PET) with 250g powder
- 25g: box (cardboard) with 40 sachets (PE/ALU/PP) each with 25g powder
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
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:
-
Belgium
Procedure number:
- BE/V/0027/001
Concerned member states:
-
Austria
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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