Veterinary Medicines

Aqupharm 1 (9 mg/ml) solution for injection/infusion

Authorised
  • Sodium chloride
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Product identification

Medicine name:
AQUPHARM SODIUM CHLORIDE 9 MG/ML SOLUTION FOR INJECTION/INFUSION
Aqupharm 1 (9 mg/ml) solution for injection/infusion
Active substance:
  • Sodium chloride
Target species:
  • Cattle
  • Pig
  • Rabbit
  • Cat
  • Horse
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Sodium chloride
    9.00
    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
        hour
    • Pig
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
    • Cat
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Dog
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
    • Cat
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Cardboard box containing 30 bags of 250 ml
  • Cardboard box containing 20 bags of 500 ml
  • Cardboard box containing 10 bags of 1000 ml
  • Cardboard box containing 4 bags of 3000 ml
  • Cardboard box containing 2 bags of 5000 ml
  • Cardboard box containing 50 bags of 100 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:
  • Infomed Fluids S.R.L.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10491/010/001
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0302/001
Concerned member states:
  • Belgium
  • Finland
  • Hungary
  • Iceland
  • Ireland
  • Netherlands
  • Sweden
  • United Kingdom (Northern Ireland)
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