Veterinary Medicines

Purevax RCPCh FeLV (--) - Lyophilisate and solvent for suspension for injection

Authorised
  • Feline calicivirus, strains 431 and G1, Inactivated
  • Chlamydophila felis, celms 905, Dzīvas
  • Feline panleukopenia virus, strain PLI IV, Live
  • Kaķu rinotraheīta vīruss, celms F2, Dzīvs
  • Canarypox virus expressing Feline leukemia virus, Live
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Identificación del producto

Nombre del medicamento:
Purevax RCPCh FeLV (--) - Lyophilisate and solvent for suspension for injection
Principio activo:
Especies de destino:
  • Gatos
Vía de administración:
  • Vía subcutánea

Datos del producto

Principio activo y concentración:
  • Disponible únicamente en English
    Presentation_strength:≥2.0 ELISA U Reference:Hse Comments:Freeze dried pellet Index:0
  • Disponible únicamente en English
    Presentation_strength:≥10³·° EID₅₀ Reference:Hse Comments:Freeze dried pellet Index:1
  • Disponible únicamente en English
    Presentation_strength:≥10³·⁵ CCID₅₀ Reference:Hse Comments:Freeze dried pellet Index:2
  • Disponible únicamente en English
    Presentation_strength:≥10⁴·⁹ CCID₅₀ Reference:Hse Comments:Freeze dried pellet Index:3
  • Disponible únicamente en English
    Presentation_strength:≥10⁷·² CCID₅₀ Reference:Hse Comments:Diluent Index:4
Forma farmacéutica:
  • Liofilizado y disolvente para suspensión inyectable
Withdrawal period by route of administration:
  • Subcutaneous use
    • Gatos
Código Anatómico Terapéutico Químico Veterinario (ATCvet):
  • QI06AX
Régimen jurídico de dispensación:
Estado de la autorización:
  • Autorizado
Authorised in:
  • Alemania
  • Austria
  • Bulgaria
  • Bélgica
  • Chipre
  • Croacia
  • Dinamarca
  • Eslovaquia
  • Eslovenia
  • España
  • Estonia
  • Finlandia
  • Francia
  • Grecia
  • Hungría
  • Irlanda
  • Islandia
  • Italia
  • Letonia
  • Liechtenstein
  • Lituania
  • Luxemburgo
  • Malta
  • Noruega
  • Países Bajos
  • Polonia
  • Portugal
  • República Checa
  • Rumania; Rumanía
  • Suecia
  • United Kingdom (Northern Ireland)
Descripción del empaquetado:

Información adicional

Entitlement type:
Fundamento jurídico de la autorización del producto:
Titular de la autorización de comercialización:
  • Boehringer Ingelheim Vetmedica GmbH
Autorización de comercialización expedida:
Centros de fabricación responsables de la liberación del lote:
  • Boehringer Ingelheim Animal Health France
País de la autorización:
No se dispone de esta información para este producto.
Autoridad responsable:
  • European Commission
Número de autorización:
No se dispone de esta información para este producto.
Fecha del cambio de estado de la autorización:

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