Parofor 140 mg/ml Solution for use in drinking water/milk
Parofor 140 mg/ml Solution for use in drinking water/milk
Authorised
- Paromomycin sulfate
Product identification
Medicine name:
Parofor 140 mg/ml Oplossing voor gebruik in het drinkwater/in de melk
Parofor 140 mg/ml Solution pour administration dans l'eau de boisson/le lait
Parofor 140 mg/ml Lösung zum Eingeben über das Trinkwasser/die Milch
Parofor 140 mg/ml Solution for use in drinking water/milk
Active substance:
- Paromomycin sulfate
Target species:
-
Cattle
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Paromomycin sulfate200.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution 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
Package description:
- Parofor 140 mg/ml sol. for drinking water/milk 1000 ml
- Parofor 140 mg/ml sol. for drinking water/milk 500 ml
- Parofor 140 mg/ml sol. for drinking water/milk 250 ml
- Parofor 140 mg/ml sol. for drinking water/milk 125 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – change in strength (Article 19(1)(a) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet J.S.C.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V513840
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0027/002
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)
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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Combined File of all Documents
English (PDF)
Download Published on: 12/07/2022
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