Veterinary Medicines

Vetivex 11 (Hartmann's) solution for infusion for cattle, horses, dogs and cats

Authorised
  • Calcium chloride dihydrate
  • Potassium chloride
  • Sodium chloride
  • Sodium lactate
Download as PDF

Product identification

Medicine name:
Vetivex 11 (Hartmann's) solution for infusion for cattle, horses, dogs and cats
Active substance:
  • Calcium chloride dihydrate
  • Potassium chloride
  • Sodium chloride
  • Sodium lactate
Target species:
  • Cattle
  • Dog
  • Horse
  • Cat
Route of administration:
  • Intravenous use

Product details

Active substance and strength:
  • Calcium chloride dihydrate
    0.27
    milligram(s)
    /
    1.00
    millilitre(s)
  • Potassium chloride
    0.40
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium chloride
    6.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium lactate
    3.20
    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
    • Dog
    • Horse
      • Meat and offal
        0
        day
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Package description:
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports. Pack size: Individual fluid bag of 250 ml, each supplied with a package leaflet.
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports.Pack size: Individual fluid bag of 500 ml, each supplied with a package leaflet
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports.Pack size: Individual fluid bag of 1000 ml, each supplied with a package leaflet
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports.Pack size: Individual fluid bag of 3000 ml, each supplied with a package leaflet
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports. In place of the additive port on the 5000 ml combipack is a combi port. This enables two such bag to be connected in sequence and volumes greater than 5000 ml to be administered during one infusion.Pack size: 5000 ml combi, each supplied with a package leaflet
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports.Pack sizes: boxes containing 20 x 250 ml
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports. Pack sizes: boxes containing 20 x 500 ml
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports.Pack sizes: boxes containing 10 x 1000 ml
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports. Pack sizes: boxes containing 4 x 3000 ml.
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports. In place of the additive port on the 5000 ml combipack is a combi port. This enables two such bags to be connected in sequence and volumes greater than 5000 ml to be administered during one infusion.Pack sizes: boxes containing 2 x 5000 ml combi.
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports. Pack sizes: boxes containing 3 x 3000 ml
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports. Pack sizes: boxes containing 15 x 500 ml
  • Polyvinylchloride infusion bags overwrapped with polypropylene.All pack sizes have two ports.Pack sizes: boxes containing 2 x 5000 ml.
  • Polyvinylchloride infusion bag overwrapped with polypropylene.All pack sizes have two ports. Pack size: Individual fluid bag of 5000 ml, each supplied with a package leaflet

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:
  • Dechra Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Industria Farmaceutica Galenica Senese S.r.l.
  • Infomed Fluids S.R.L.
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • 10434/4080
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0512/001
Concerned member states:
  • Belgium
  • Denmark
  • France
  • Germany
  • Netherlands
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."