- Application under evaluation
- CVMP opinion
- European Commission decision
Overview
The marketing authorisation for Purevax RCCh has lapsed because it has not been marketed in the European Union in the three years following the granting of the authorisation.
Purevax RCCh : EPAR - Summary for the public
English (EN) (1.07 MB - PDF)
български (BG) (1.23 MB - PDF)
español (ES) (1.07 MB - PDF)
čeština (CS) (1.17 MB - PDF)
dansk (DA) (1.08 MB - PDF)
Deutsch (DE) (1.08 MB - PDF)
eesti keel (ET) (1.08 MB - PDF)
ελληνικά (EL) (1.18 MB - PDF)
français (FR) (1.08 MB - PDF)
italiano (IT) (1.08 MB - PDF)
latviešu valoda (LV) (1.16 MB - PDF)
lietuvių kalba (LT) (1.17 MB - PDF)
magyar (HU) (1.16 MB - PDF)
Malti (MT) (1.17 MB - PDF)
Nederlands (NL) (1.07 MB - PDF)
polski (PL) (1.18 MB - PDF)
português (PT) (1.08 MB - PDF)
română (RO) (1.17 MB - PDF)
slovenčina (SK) (1.17 MB - PDF)
slovenščina (SL) (1.15 MB - PDF)
Suomi (FI) (1.07 MB - PDF)
svenska (SV) (1.07 MB - PDF)
Product information
Purevax RCCh : EPAR - Product Information
English (EN) (269.91 KB - PDF)
български (BG) (374.27 KB - PDF)
español (ES) (279.48 KB - PDF)
čeština (CS) (356.65 KB - PDF)
dansk (DA) (278.12 KB - PDF)
Deutsch (DE) (348.87 KB - PDF)
eesti keel (ET) (271.16 KB - PDF)
ελληνικά (EL) (376.47 KB - PDF)
français (FR) (271.82 KB - PDF)
italiano (IT) (280.06 KB - PDF)
latviešu valoda (LV) (367.85 KB - PDF)
lietuvių kalba (LT) (172.31 KB - PDF)
magyar (HU) (359.84 KB - PDF)
Malti (MT) (373.08 KB - PDF)
Nederlands (NL) (277.75 KB - PDF)
polski (PL) (382.15 KB - PDF)
português (PT) (113.33 KB - PDF)
română (RO) (171.68 KB - PDF)
slovenčina (SK) (367.23 KB - PDF)
slovenščina (SL) (354.17 KB - PDF)
Suomi (FI) (274.18 KB - PDF)
svenska (SV) (271.32 KB - PDF)
Purevax RCCh : EPAR - All Authorised presentations
English (EN) (1.02 MB - PDF)
български (BG) (656.37 KB - PDF)
español (ES) (1.03 MB - PDF)
čeština (CS) (644.91 KB - PDF)
dansk (DA) (593.89 KB - PDF)
Deutsch (DE) (600.45 KB - PDF)
eesti keel (ET) (587.75 KB - PDF)
ελληνικά (EL) (808.99 KB - PDF)
français (FR) (588.65 KB - PDF)
íslenska (IS) (594.57 KB - PDF)
italiano (IT) (596.67 KB - PDF)
latviešu valoda (LV) (641.54 KB - PDF)
lietuvių kalba (LT) (637.85 KB - PDF)
magyar (HU) (619.22 KB - PDF)
Malti (MT) (648.17 KB - PDF)
Nederlands (NL) (599.84 KB - PDF)
norsk (NO) (598.77 KB - PDF)
polski (PL) (1.07 MB - PDF)
português (PT) (600.34 KB - PDF)
română (RO) (645.37 KB - PDF)
slovenčina (SK) (644.69 KB - PDF)
slovenščina (SL) (625.67 KB - PDF)
Suomi (FI) (587.85 KB - PDF)
svenska (SV) (588.17 KB - PDF)
Product details
- Name of medicine
- Purevax RCCh
- Active substance
- attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
- inactivated feline calicivirosis antigens (FCV 431 and G1 strains)
- attenuated Chlamydophila felis (905 strain)
- International non-proprietary name (INN) or common name
- vaccine against feline viral rhinotracheitis, feline calicivirosis and feline Chlamydophila infections
- Species
- Cats
- Anatomical therapeutic chemical veterinary (ATCvet) code
- QI06AH
Pharmacotherapeutic group
Immunologicals for felidaeTherapeutic indication
Active immunisation of cats aged 8 weeks and older:
- against feline viral rhinotracheitis to reduce clinical signs;
- against calicivirus infection to reduce clinical signs and excretion;
- against Chlamydophila felis infection to reduce clinical signs.
Onsets of immunity have been demonstrated 1 week after primary vaccination course for rhinotracheitis, calicivirus and Chlamydophila felis components.
The duration of immunity is 1 year after the last (re-)vaccination.
Authorisation details
- EMA product number
- EMEA/V/C/000092
- Marketing authorisation holder
- Merial
29 Avenue Tony Garnier
69007 Lyon
France - Marketing authorisation issued
- 22/02/2005
- Lapse of marketing authorisation
- 22/02/2008
- Revision
- 8
Assessment history
Purevax RCCh : EPAR - Procedural steps taken and scientific information after authorisation
English (EN) (159.61 KB - PDF)