Syvazul BTV BTV 1 - Suspension for injection
Syvazul BTV BTV 1 - Suspension for injection
Authorised
- Bluetongue virus, serotype 1, strain ALG2006/01 E1, Inactivated
Product identification
Medicine name:
Syvazul BTV BTV 1 - Suspension for injection
Active substance:
- Bluetongue virus, serotype 1, strain ALG2006/01 E1, Inactivated
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Bluetongue virus, serotype 1, strain ALG2006/01 E1, InactivatedPresentation_strength:RP ≥ 1 Reference:Hse Index:0
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Not applicable0dayZero days
-
- Sheep
-
Not applicable0dayZero days
-
-
Subcutaneous use
- Cattle
-
Not applicable0dayZero days
-
- Sheep
-
Not applicable0dayZero days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Liechtenstein
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Available in:
-
Spain
Package description:
- Packaging:Vial (PP), Package_size:1 vial, Content:200 ml (100 sheep doses or 50 cattle doses)
- Packaging:Vial (PP), Package_size:1 vial, Content:80 ml (40 sheep doses or 20 cattle doses)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Laboratorios Syva S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Syva S.A.U.
Responsible authority:
- European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 28/07/2023
Bulgarian (PDF)
Published on: 28/07/2023
Croatian (PDF)
Published on: 28/07/2023
Danish (PDF)
Published on: 28/07/2023
Greek (PDF)
Published on: 28/07/2023
Hungarian (PDF)
Published on: 28/07/2023
Norwegian (PDF)
Published on: 28/07/2023
Spanish (PDF)
Published on: 28/07/2023
ema-puar-syvazul-btv-v-4611-par-en.pdf
English (PDF)
Download Published on: 16/03/2023
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