Veterinary Medicines

URSOFERRAN 200 mg/ml Solution for injection for pigs

Authorised
  • Gleptoferron
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Product identification

Medicine name:
URSOFERRAN 200 mg/ml Solution for injection for pigs
Viloferron 200 mg/ml injektionsvæske, opløsning
Active substance:
  • Gleptoferron
Target species:
  • Pig (suckling piglet)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Gleptoferron
    532.60
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (suckling piglet)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB03AC
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:
  • (ID6) 2000 millilitre(s): unspecified outer container with 10 Vial (low-density polyethylene) each with 200 millilitre(s)
  • (ID5) 200 millilitre(s): unspecified outer container with 1 Vial (low-density polyethylene) with 200 millilitre(s)
  • (ID4) 1000 millilitre(s): unspecified outer container with 10 Vial (low-density polyethylene) each with 100 millilitre(s)
  • (ID3) 1000 millilitre(s): unspecified outer container with 10 Vial (glass) each with 100 millilitre(s)
  • (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (low-density polyethylene) with 100 millilitre(s)
  • (ID1) 100 millilitre(s): unspecified outer container with 1 Vial (glass) with 100 millilitre(s)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Serumwerk Bernburg AG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Serumwerk Bernburg AG
  • Ceva Sante Animale
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 51985
Reference member state:
  • Germany
Procedure number:
  • DE/V/0149/001
Concerned member states:
  • Belgium
  • Czechia
  • Denmark
  • Finland
  • France
  • Hungary
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Danish (, INJEKTIONSVÆSKE, OPLØSNING 200 MG-ML)
Published on: 17/07/2023
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Combined File of all Documents

English (PDF)
Published on: 12/01/2026
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3100349-paren-20181018.rtf

English (RTF)
Published on: 12/01/2026
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