Veterinary Medicine Information website

Enro-Sleecol 100 mg/ml oral solution for chickens and turkeys

Authorised

Enrofloxacin

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Product identification

Medicine name:

Enro-Sleecol 100 mg/ml oral solution for chickens and turkeys

Active substance:

Enrofloxacin

Target species:

Turkey
Chicken

Route of administration:

In drinking water use

Product details

Active substance and strength:

Enrofloxacin

100.00

milligram(s)

/

1.00

millilitre(s)

Pharmaceutical form:

Oral solution

Withdrawal period by route of administration:

In drinking water use
- Turkey
  - Meat and offal
    
    13
    
    day
  - Egg
    
    no withdrawal period
    
    Not authorised for use in laying birds producing eggs for human consumption.
- Chicken
  - Egg
    
    no withdrawal period
    
    Not authorised for use in laying birds producing eggs for human consumption. Do not administer to layer replacement birds within 14 days of coming into lay.
  - Meat and offal
    
    7
    
    day

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 (high-density polyethylene) with 5 litre(s)
(ID2) 1 litre(s): unspecified outer container with 1 Bottle (high-density polyethylene) with 1 litre(s)
(ID1) 100 millilitre(s): unspecified outer container with 1 Bottle (brown glass) 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:

23/03/2011

Manufacturing sites for batch release:

KRKA tovarna zdravil d.d. Novo mesto

Responsible authority:

Federal Agency For Medicines And Health Products

Authorisation number:

This information is not available for this product.

Date of authorisation status change:

23/03/2011

Reference member state:

Germany

Procedure number:

DE/V/0335/001

Concerned member states:

Belgium

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 18/08/2025

German (PDF)

Published on: 18/08/2025

Dutch (PDF)

Published on: 18/08/2025

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 18/08/2025

German (PDF)

Published on: 18/08/2025

Dutch (PDF)

Published on: 18/08/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.

Other languages (3)

French (PDF)

Published on: 18/08/2025

German (PDF)

Published on: 18/08/2025

Dutch (PDF)

Published on: 18/08/2025

Combined File of all Documents

English (PDF)

Published on: 11/03/2026

2401361-paren-20190801.rtf

English (RTF)

Published on: 11/03/2026