Canigen L4 (--) - Suspension for injection
Canigen L4 (--) - Suspension for injection
Authorised
- Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
- Leptospira interrogans, serovar Bratislava, strain As-05-073, Inactivated
- Leptospira kirschneri, serovar Dadas, strain GR-01-005, Inactivated
Product identification
Medicine name:
Canigen L4 (--) - Suspension for injection
Active substance:
- Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
- Leptospira interrogans, serovar Bratislava, strain As-05-073, Inactivated
- Leptospira kirschneri, serovar Dadas, strain GR-01-005, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, InactivatedPresentation_strength:3550-7100 U Reference:Hse Index:0
-
Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, InactivatedPresentation_strength:290-1000 U Reference:Hse Index:1
-
Leptospira interrogans, serovar Bratislava, strain As-05-073, InactivatedPresentation_strength:500-1700 U Reference:Hse Index:2
-
Leptospira kirschneri, serovar Dadas, strain GR-01-005, InactivatedPresentation_strength:650-1300 U Reference:Hse Index:3
Pharmaceutical form:
-
Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AB01
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
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Latvia
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Liechtenstein
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Lithuania
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Luxembourg
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Malta
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Netherlands
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Norway
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Poland
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Portugal
-
Romania
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Slovakia
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Slovenia
-
Spain
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Sweden
-
United Kingdom (Northern Ireland)
Available in:
-
France
-
Norway
-
Poland
-
Spain
Package description:
- Packaging:Vial (glass), Package_size:50 vials, Content:1 ml (1 dose)
- Packaging:Vial (glass), Package_size:10 vials, Content:1 ml (1 dose)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
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: 1/09/2023
Romanian (PDF)
Published on: 1/09/2023
Slovenian (PDF)
Published on: 1/09/2023
Portuguese (PDF)
Published on: 1/09/2023
Dutch (PDF)
Published on: 1/09/2023
Polish (PDF)
Published on: 1/09/2023
Danish (PDF)
Published on: 1/09/2023
Spanish (PDF)
Published on: 1/09/2023
Greek (PDF)
Published on: 1/09/2023
Norwegian (PDF)
Published on: 1/09/2023
Czech (PDF)
Published on: 1/09/2023
Bulgarian (PDF)
Published on: 1/09/2023
Estonian (PDF)
Published on: 1/09/2023
German (PDF)
Published on: 1/09/2023
Maltese (PDF)
Published on: 1/09/2023
Slovak (PDF)
Published on: 1/09/2023
Swedish (PDF)
Published on: 1/09/2023
French (PDF)
Published on: 1/09/2023
Icelandic (PDF)
Published on: 1/09/2023
Hungarian (PDF)
Published on: 1/09/2023
Lithuanian (PDF)
Published on: 1/09/2023
Italian (PDF)
Published on: 1/09/2023
Finnish (PDF)
Published on: 1/09/2023
Croatian (PDF)
Published on: 1/09/2023
Latvian (PDF)
Published on: 1/09/2023
ema-puar-canigen-v-4079-par-en.pdf
English (PDF)
Download Published on: 13/03/2023
