Veterinary Medicines

ANAESTAMINE 100 MG/ML SOLUTION FOR INJECTION

Authorised
  • Ketamine hydrochloride
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Product identification

Medicine name:
ANAESTAMINE 100 MG/ML SOLUTION FOR INJECTION
Aniketam 100 mg/ml, injekcinis tirpalas
Active substance:
  • Ketamine hydrochloride
Target species:
  • Cattle
  • Pig
  • Rat
  • Mouse
  • Hamster
  • Guinea pig
  • Rabbit
  • Cat
  • Horse
  • Horse (mare)
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Intraperitoneal use

Product details

Active substance and strength:
  • Ketamine hydrochloride
    115.34
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Horse (mare)
      • Milk
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        1
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        1
        day
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
    • Horse (mare)
      • Milk
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        1
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01AX03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Lithuania
Package description:
  • Vial containing 10 ml in a carton box
  • Vial containing 50 ml in a carton box
  • Vial containing 25 ml in a carton box

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:
  • Le Vet. Beheer B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Produlab Pharma B.V.
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/14/2240/001-003
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0262/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

RV2240.pdf

Lithuanian (PDF)
Published on: 10/05/2022
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