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
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 chloride9.00/milligram(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
-
-
Cattle
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Horse
-
Meat and offal0day0 days
-
Milk0day0 days
-
-
Pig
-
Meat and offal0day0 days
-
-
-
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
-
-
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
Available 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
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Package Leaflet
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Labelling
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