Sodium Chloride 0.9 g/100 ml B. Braun Vet Care solution for infusion for cattle, horse, sheep, goat, pig, dog and cat
Sodium Chloride 0.9 g/100 ml B. Braun Vet Care solution for infusion for cattle, horse, sheep, goat, pig, dog and cat
Authorised
- Sodium chloride
Product identification
Medicine name:
Sodium Chloride 0.9 g/100 ml B. Braun Vet Care solution for infusion for cattle, horse, sheep, goat, pig, dog and cat
Chlorure de Sodium 0,9 g/100 ml B. Braun Vet Care Oplossing voor infusie
Chlorure de Sodium 0,9 g/100 ml B. Braun Vet Care Solution pour perfusion
Chlorure de Sodium 0,9 g/100 ml B. Braun Vet Care Infusionslösung
Active substance:
- Sodium chloride
Target species:
-
Cattle
-
Horse
-
Sheep
-
Goat
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intravenous use
Product details
Active substance and strength:
-
Sodium chloride0.90gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for infusion
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Horse
-
Sheep
-
Goat
-
Pig
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB05BB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Polyethylene bottles Polyethylene bottles 10 bottles with 1000 ml solution for infusion
- Polyethylene bottles 10 bottles with 500 ml solution for infusion
- Polyethylene bottles 20 bottles with 100 ml solution for infusion
- Polyethylene bottles Polyethylene bottles 20 bottles with 250 ml solution for infusion
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- B. Braun Melsungen AG
Marketing authorisation date:
Manufacturing sites for batch release:
- B. Braun Melsungen AG
- B BRAUN MEDICAL S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V444202
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0115/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
France
-
Germany
-
Ireland
-
Italy
-
Netherlands
-
Poland
-
Romania
-
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
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Package Leaflet
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Labelling
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