Vetivex 11 (Hartmann's) solution for infusion for cattle, horses, dogs and cats
Vetivex 11 (Hartmann's) solution for infusion for cattle, horses, dogs and cats
Authorised
- Calcium chloride dihydrate
- Potassium chloride
- Sodium chloride
- Sodium lactate
Product identification
Medicine name:
Vetivex 11 (Hartmann's) solution for infusion for cattle, horses, dogs and cats
Infusolec Infusionsvätska, lösning
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 dihydrate0.27milligram(s)1.00millilitre(s)
-
Potassium chloride0.40milligram(s)1.00millilitre(s)
-
Sodium chloride6.00milligram(s)1.00millilitre(s)
-
Sodium lactate3.20milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Dog
- Horse
-
Meat and offal0day
-
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05BB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Package description:
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
- Available only in Swedish
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 Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Industria Farmaceutica Galenica Senese S.r.l.
- Infomed Fluids S.R.L.
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 48074
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)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
Swedish (PDF)
Published on: 16/08/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 15/08/2023
How useful was this page?: