Veterinary Medicines

AQUPHARM RINGER LACTATE SOLUTION FOR INFUSION

Authorised
  • Sodium chloride
  • Sodium lactate
  • Calcium chloride
  • Potassium chloride
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Product identification

Medicine name:
AQUPHARM RINGER LACTATE SOLUTION FOR INFUSION
Aqupharm ringerlactaat oplossing voor infusie
Active substance:
  • Sodium chloride
  • Sodium lactate
  • Calcium chloride
  • Potassium chloride
Target species:
  • Cattle
  • Pig
  • Rabbit
  • Cat
  • Horse
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intravenous use

Product details

Active substance and strength:
  • Sodium chloride
    6.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium lactate
    3.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium chloride
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Potassium chloride
    0.40
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • 1 bag of 250 ml
  • 1 bag of 500 ml
  • 1 bag of 1000 ml
  • 1 bag of 3000 ml
  • 1 bag of 5000 ml
  • Cardboard box containing 30 bags of 250 ml
  • Cardboard box containing 2 bags of 5000 ml
  • Cardboard box containing 4 bags of 3000 ml
  • Cardboard box containing 10 bags of 1000 ml
  • Cardboard box containing 20 bags of 500 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
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratoire Bioluz
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 117955
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0303/001
Concerned member states:
  • Belgium
  • Finland
  • Hungary
  • Iceland
  • Ireland
  • Netherlands
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 18/11/2025
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