Nobivac NXT HCPCh (--) + (--) + (--) + (--) - Lyophilisate and solvent for suspension for injection
Nobivac NXT HCPCh (--) + (--) + (--) + (--) - Lyophilisate and solvent for suspension for injection
Authorised
- Felid herpesvirus 1, strain G2620A, Live
- Feline calicivirus, strain F9, Live
- Feline panleucopenia virus, strain MW-1, Live
- Chlamydia felis, strain Baker, Live
Product identification
Medicine name:
Nobivac NXT HCPCh (--) + (--) + (--) + (--) - Lyophilisate and solvent for suspension for injection
Active substance:
- Felid herpesvirus 1, strain G2620A, Live
- Feline calicivirus, strain F9, Live
- Feline panleucopenia virus, strain MW-1, Live
- Chlamydia felis, strain Baker, Live
Target species:
-
Cat
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Felid herpesvirus 1, strain G2620A, LivePresentation_strength:10⁵·⁸ – 10⁷·¹ PFU Index:0
-
Feline calicivirus, strain F9, LivePresentation_strength:10⁴·⁶ – 10⁷·⁰ PFU Index:1
-
Feline panleucopenia virus, strain MW-1, LivePresentation_strength:10⁵·² – 10⁶·⁴ TCID₅₀ Index:2
-
Chlamydia felis, strain Baker, LivePresentation_strength:10⁴·¹ – 10⁷·⁰ TCID₅₀ Index:3
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI06AF01
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
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Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
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Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Package description:
- Packaging:Vial (glass), Package_size:Lyophilisate: 25 vials + solvent: 25 vials, Content:Lyophilisate: 1 dose + solvent: 0.5 ml
- Packaging:Vial (glass), Package_size:Lyophilisate: 5 vials + solvent: 5 vials, Content:Lyophilisate: 1 dose + solvent: 0.5 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
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: 25/08/2026
Maltese (PDF)
Published on: 25/08/2026
Estonian (PDF)
Published on: 25/08/2026
Croatian (PDF)
Published on: 25/08/2026
Finnish (PDF)
Published on: 25/08/2026
Spanish (PDF)
Published on: 25/08/2026
Dutch (PDF)
Published on: 25/08/2026
German (PDF)
Published on: 25/08/2026
Hungarian (PDF)
Published on: 25/08/2026
Bulgarian (PDF)
Published on: 25/08/2026
Icelandic (PDF)
Published on: 25/08/2026
Greek (PDF)
Published on: 25/08/2026
Latvian (PDF)
Published on: 25/08/2026
Norwegian (PDF)
Published on: 25/08/2026
Lithuanian (PDF)
Published on: 25/08/2026
French (PDF)
Published on: 25/08/2026
Danish (PDF)
Published on: 25/08/2026
Italian (PDF)
Published on: 25/08/2026
Czech (PDF)
Published on: 25/08/2026
Polish (PDF)
Published on: 25/08/2026
Portuguese (PDF)
Published on: 25/08/2026
Romanian (PDF)
Published on: 25/08/2026
Slovak (PDF)
Published on: 25/08/2026
Slovenian (PDF)
Published on: 25/08/2026
Swedish (PDF)
Published on: 25/08/2026
