Enrotron 100, 100 mg/ml solution for injection for cattle and pigs
Enrotron 100, 100 mg/ml solution for injection for cattle and pigs
Authorised
- Enrofloxacin
Product identification
Medicine name:
Enrotron 100, 100 mg/ml solution for injection for cattle and pigs
Active substance:
- Enrofloxacin
Target species:
-
Cattle
-
Goat
-
Sheep
-
Pig
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat and offal5day
-
Milk72hour
-
-
-
Subcutaneous use
-
Goat
-
Meat and offal6day
-
Milk96hour
-
-
Sheep
-
Meat and offal4day
-
Milk72hour
-
-
Cattle
-
Meat and offal12day
-
Milk96hour
-
-
-
Intramuscular use
-
Pig
-
Meat and offal13day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Available in:
-
Austria
Package description:
- Available only in German
- Available only in German
- (ID4) 3000 millilitre(s): unspecified outer container with 12 Vial (glass) each with 250 millilitre(s), closed with Stopfen (rubber)
- (ID3) 250 millilitre(s): unspecified outer container with 1 Vial (glass) with 250 millilitre(s), closed with Stopfen (rubber)
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:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-01122
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0147/003
Concerned member states:
-
Austria
-
Slovenia
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.
German (PDF)
Published on: 25/09/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 25/09/2025
Labelling
This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 25/09/2025
Combined File of all Documents
English (PDF)
Download Published on: 12/12/2025
2401622-paren-20180221.rtf
English (RTF)
Download Published on: 12/12/2025