Veterinary Medicines Information website

HEMOSILATE 125 mg/ml solution for injection

Authorised
  • Etamsilate
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Product identification

Medicine name:
HEMOSILATE 125 mg/ml solution for injection
Active substance:
  • Etamsilate
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Horse
  • Dog
  • Cat
Route of administration:
  • Intravenous use
  • Intramuscular use

Product details

Active substance and strength:
  • Etamsilate
    125.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Goat
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Pig
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Goat
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
    • Pig
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB02BX01
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 10 vials of 20 ml
  • cardboard box containing 5 vials of 20 ml
  • cardboard box containing 1 vial of 20 ml

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:
  • Ecuphar Veterinaria S.L.U.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 402660.00.00
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0281/001
Concerned member states:
  • Austria
  • Belgium
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 27/04/2026
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eu-PUAR-esv0281001-dcp-hemosilate-125-mg-ml-solution-for-injection-en.pdf

English (PDF)
Published on: 14/03/2026
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