Veterinary Medicines

Fysiologische zoutoplossing, 9 mg/ml, oplossing voor injectie

Authorised
  • Sodium chloride
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Product identification

Medicine name:
Fysiologische zoutoplossing, 9 mg/ml, oplossing voor injectie
Active substance:
  • Sodium chloride
Target species:
  • Ruminant
  • Equid
  • Pig
  • Fowl
  • Carnivores
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 injection
Withdrawal period by route of administration:
  • Intravenous use
    • Ruminant
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Equid
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Fowl
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
  • Subcutaneous use
    • Ruminant
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Equid
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
    • Fowl
      • Meat and offal
        no withdrawal period
      • Egg
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05XA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Bruin glazen flacon (type II) á 500 ml, afgesloten met een broombutyl rubberstop en aluminium felscapsule.
  • Bruin glazen flacon (type II) á 100 ml, afgesloten met een broombutyl rubberstop en aluminium felscapsule.
  • Bruin glazen flacon (type II) á 750 ml, afgesloten met een broombutyl rubberstop en aluminium felscapsule.
  • Bruin glazen flacon (type II) á 10 liter, afgesloten met een broombutyl rubberstop en aluminium felscapsule.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 1247
Date of authorisation status change:

Documents

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Dutch (PDF)
Published on: 15/02/2022
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