Enrotron 100 mg/ml oral solution for chicken and turkeys
Enrotron 100 mg/ml oral solution for chicken and turkeys
Authorised
- Enrofloxacin
Product identification
Medicine name:
Enrotron 100 mg/ml oral solution for chicken and turkeys
Enrotron 100 mg/ml
Active substance:
- Enrofloxacin
Target species:
-
Turkey
-
Rabbit
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Enrofloxacin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal13day
-
-
Rabbit
-
Meat and offal15day
-
-
Chicken
-
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:
-
Germany
Available in:
-
Germany
Package description:
- Cardboard box containing 6 x 1000 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.
- Cardboard box containing 12 x 100 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.
- 1000 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher
- Cardboard box containing 100 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.
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:
- aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- aniMedica GmbH
- Industrial Veterinaria S.A.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401661.00.00
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0165/003
Concerned member states:
-
Cyprus
-
France
-
Germany
-
Ireland
-
Poland
-
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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in another language below.
German (RTF)
Published on: 20/12/2024
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