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, oplossing voor injectie
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
  • 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
  • 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:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • (ID4): 1 unspecified outer container with 12 Vial (Glass) with 50 millilitre(s) (600 millilitre(s))
  • (ID3): 1 unspecified outer container with 1 Vial (Glass) with 50 millilitre(s) (50 millilitre(s))
  • (ID2): 1 unspecified outer container with 12 Vial (Glass) with 100 millilitre(s) (1200 millilitre(s))
  • (ID1): 1 unspecified outer container with 1 Vial (Glass) with 100 millilitre(s) (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:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 101841
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

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 8/02/2022
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Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
Download
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