Veterinary Medicines

Release 300 mg/ml, solution for injection

Authorised
  • Pentobarbital sodium
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Product identification

Medicine name:
Release 300 mg/ml, solution for injection
Release 300 mg/ml soluzione iniettabile
Active substance:
  • Pentobarbital sodium
Target species:
  • Dog
  • Cat
  • Hare
  • Rabbit
  • Guinea pig
  • Hamster
  • Mouse
  • Rat
  • Pigeon
  • Cattle
  • Chicken
  • Ornamental bird
  • Horse (pony)
  • Mink
  • Polecat
  • Pig
  • Horse (non food-producing)
  • Frog
  • Lizard
  • Snake
  • Turtle
Route of administration:
  • Intraperitoneal use
  • Intravenous use
  • Intracardiac use
  • Intrapulmonary use

Product details

Active substance and strength:
  • Pentobarbital sodium
    300.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Dog
    • Cat
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
  • Intravenous use
    • Pigeon
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Ornamental bird
    • Dog
    • Horse (pony)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Cat
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Mink
    • Polecat
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
    • Pig
      • Meat and offal
        no withdrawal period
    • Horse (non food-producing)
  • Intracardiac use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Dog
    • Horse (pony)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Cat
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Mink
    • Polecat
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
    • Pig
      • Meat and offal
        no withdrawal period
  • Intrapulmonary use
    • Pigeon
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Frog
    • Lizard
    • Snake
    • Turtle
    • Chicken
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
    • Ornamental bird
    • Dog
    • Cat
    • Hare
      • Meat and offal
        no withdrawal period
    • Rabbit
      • Meat and offal
        no withdrawal period
    • Mink
    • Polecat
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN51AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:
  • (ID4) 600 millilitre(s): unspecified outer container with 12 Vial (Glass) each with 50 millilitre(s)
  • (ID3) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s)
  • (ID2) 1200 millilitre(s): unspecified outer container with 12 Vial (Glass) each 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:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 104714
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0125/001
Concerned member states:
  • Austria
  • Belgium
  • Hungary
  • Ireland
  • Italy
  • Netherlands
  • Portugal
  • Spain
  • 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.
Italian (PDF)
Published on: 15/04/2025
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Combined File of all Documents

English (PDF)
Published on: 24/07/2024
Download
Italian (PDF)
Published on: 15/04/2025
Download
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