Enroxal 100 mg/ml oral solution for chickens and turkeys
Enroxal 100 mg/ml oral solution for chickens and turkeys
Authorised
- Enrofloxacin
Product identification
Medicine name:
Enroxal 100 mg/ml oral solution for chickens and turkeys
Enroxal 100 mg/ml Drank
Enroxal 100 mg/ml Solution buvable
Enroxal 100 mg/ml Lösung zum Einnehmen
Active substance:
- Enrofloxacin
Target species:
-
Turkey
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal13day
-
Eggno withdrawal periodNot authorised for use in birds producing eggs for human consumption. Do not administer to layer replacement birds within 14 days of coming into lay.
-
-
Chicken
-
Eggno withdrawal periodNot authorised for use in birds producing eggs for human consumption. Do not administer to layer replacement birds within 14 days of coming into lay.
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- (ID3) 5 litre(s): unspecified outer container with 1 Bottle (Polyethylen hoher Dichte) with 5 litre(s)
- (ID2) 1 litre(s): unspecified outer container with 1 Bottle (Polyethylen hoher Dichte) with 1 litre(s)
- (ID1) 100 millilitre(s): unspecified outer container with 1 Bottle (Braunglas) with 100 millilitre(s)
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:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
- TAD Pharma GmbH
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:
-
Germany
Procedure number:
- DE/V/0336/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Cyprus
-
Italy
-
Netherlands
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: 21/08/2024
Labelling
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