Etosol-Se 50 mg/ml - 987 mg/ml Oplossing voor injectie
Etosol-Se 50 mg/ml - 987 mg/ml Oplossing voor injectie
Authorised
- Sodium selenite
- alfa-Tocopheryl acetate
Product identification
Medicine name:
Etosol-Se 50 mg/ml - 987 mg/ml Oplossing voor injectie
Active substance:
- Sodium selenite
- alfa-Tocopheryl acetate
Target species:
-
Cattle (calf)
-
Cattle
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Sodium selenite0.99/milligram(s)1.00millilitre(s)
-
alfa-Tocopheryl acetate50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle (calf)
-
Meat and offal15dayFrench:Viande et abats : 15 jours. ; Dutch:Vlees en slachtafval: 15 dagen.
-
-
-
Intramuscular use
-
Cattle
-
Meat and offal15day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11JB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Etosol-Se 100 ml Vial 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-V108832
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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