Veterinary Medicines Information website

Enrotron 100, 100 mg/ml solution for injection for cattle and pigs

Authorised
  • Enrofloxacin
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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:
  • Enrofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        5
        day
      • Milk
        72
        hour
  • Subcutaneous use
    • Goat
      • Meat and offal
        6
        day
      • Milk
        96
        hour
    • Sheep
      • Meat and offal
        4
        day
      • Milk
        72
        hour
    • Cattle
      • Meat and offal
        12
        day
      • Milk
        96
        hour
  • Intramuscular use
    • Pig
      • Meat and offal
        13
        day
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:
  • (ID2) 1200 millilitre(s): unspecified outer container with 12 Vial (glass) each with 100 millilitre(s), closed with Stopfen (rubber)
  • (ID1) 100 millilitre(s): unspecified outer container with 1 Vial (glass) with 100 millilitre(s), closed with Stopfen (rubber)
  • (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:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 401622.00.00
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0147/003
Concerned member states:
  • Austria
  • Slovenia

Documents

Combined File of all Documents

English (PDF)
Published on: 30/09/2025
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German (PDF)
Published on: 30/09/2025
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2401622-paren-20180221.rtf

English (RTF)
Published on: 25/07/2025
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