Veterinary Medicines

Doxapram-V 20 mg/ml Injektionslösung für Pferd, Fohlen, Kalb, Lamm, Hund, Katze, Zootiere

Authorised
  • Doxapram hydrochloride
Download as PDF

Product identification

Medicine name:
Doxapram-V 20 mg/ml Injektionslösung für Pferd, Fohlen, Kalb, Lamm, Hund, Katze, Zootiere
Active substance:
  • Doxapram hydrochloride
Target species:
  • Sheep (lamb)
  • Horse (foal)
  • Dog
  • Cattle (calf)
  • Cat
  • Zoo animals
  • Horse
Route of administration:
  • Subcutaneous use
  • Intravenous use
  • Oromucosal use
  • Intramuscular use

Product details

Active substance and strength:
  • Doxapram hydrochloride
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep (lamb)
      • Meat and offal
        2
        day
    • Cattle (calf)
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        2
        day
  • Intravenous use
    • Cattle (calf)
      • Meat and offal
        2
        day
    • Sheep (lamb)
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        2
        day
  • Oromucosal use
    • Sheep (lamb)
      • Meat and offal
        2
        day
    • Cattle (calf)
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        2
        day
  • Intramuscular use
    • Cattle (calf)
      • Meat and offal
        2
        day
    • Sheep (lamb)
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        2
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QR07AB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Dechra Veterinary Products Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dechra Veterinary Products Deutschland GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 5737.00.00
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (RTF)
Published on: 2/09/2024
Download

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: 2/09/2024
Download