Fysiologische Zoutoplossing Dechra Oplossing voor injectie
Fysiologische Zoutoplossing Dechra Oplossing voor injectie
Authorised
- Sodium chloride
Product identification
Medicine name:
Fysiologische Zoutoplossing Dechra Oplossing voor injectie
Fysiologische Zoutoplossing Dechra Solution injectable
Fysiologische Zoutoplossing Dechra Injektionslösung
Active substance:
- Sodium chloride
Target species:
-
Horse (foal)
-
Cattle (calf)
-
Cat
-
Cattle
-
Horse
-
Pig
-
Dog
Route of administration:
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Sodium chloride9.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Horse (foal)
-
Meat and offal0day
-
-
Cattle (calf)
-
Meat and offal0day
-
-
Cat
-
Cattle
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Horse
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Pig
-
Meat and offal0day0 days
-
-
Dog
-
-
Subcutaneous use
-
Cattle (calf)
-
Meat and offal0day
-
-
Horse (foal)
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Pig
-
Meat and offal0day0 days
-
-
Horse
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05XA03
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Fysiologische Zoutoplossing Dechra 1 Vial with 10 l of Solution for injection
- Fysiologische Zoutoplossing Dechra 1 Vial with 1 l of Solution for injection
- Fysiologische Zoutoplossing Dechra 1 Vial with 750 ml of Solution for injection
- Fysiologische Zoutoplossing Dechra 1 Vial with 500 ml of Solution for injection
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Dechra Veterinary Products
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V288294
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
How useful was this page?: