- Application under evaluation
- CVMP opinion
- European Commission decision
Overview
The marketing authorisation for Nobivac Piro has been withdrawn at the request of the marketing-authorisation holder.
Nobivac Piro : EPAR - Summary for the public
English (EN) (514.2 KB - PDF)
български (BG) (623.96 KB - PDF)
español (ES) (517.22 KB - PDF)
čeština (CS) (603.97 KB - PDF)
dansk (DA) (513.68 KB - PDF)
Deutsch (DE) (520.41 KB - PDF)
eesti keel (ET) (512.62 KB - PDF)
ελληνικά (EL) (627.36 KB - PDF)
français (FR) (513.51 KB - PDF)
italiano (IT) (515.38 KB - PDF)
latviešu valoda (LV) (599.43 KB - PDF)
lietuvių kalba (LT) (598.49 KB - PDF)
magyar (HU) (595.88 KB - PDF)
Malti (MT) (620.17 KB - PDF)
Nederlands (NL) (514.6 KB - PDF)
polski (PL) (613.03 KB - PDF)
português (PT) (515.53 KB - PDF)
română (RO) (596.07 KB - PDF)
slovenčina (SK) (602.34 KB - PDF)
slovenščina (SL) (585.83 KB - PDF)
Suomi (FI) (514.11 KB - PDF)
svenska (SV) (513.89 KB - PDF)
Product information
Nobivac Piro : EPAR - Product Information
English (EN) (542.72 KB - PDF)
български (BG) (618.96 KB - PDF)
español (ES) (518.88 KB - PDF)
čeština (CS) (624.87 KB - PDF)
dansk (DA) (515.6 KB - PDF)
Deutsch (DE) (519.99 KB - PDF)
eesti keel (ET) (531.06 KB - PDF)
ελληνικά (EL) (618.69 KB - PDF)
français (FR) (513.56 KB - PDF)
italiano (IT) (538.08 KB - PDF)
latviešu valoda (LV) (603.69 KB - PDF)
lietuvių kalba (LT) (602.15 KB - PDF)
magyar (HU) (590.63 KB - PDF)
Malti (MT) (610.8 KB - PDF)
Nederlands (NL) (532.11 KB - PDF)
polski (PL) (634.94 KB - PDF)
português (PT) (535.76 KB - PDF)
română (RO) (609.2 KB - PDF)
slovenčina (SK) (628.87 KB - PDF)
slovenščina (SL) (587.55 KB - PDF)
Suomi (FI) (514.44 KB - PDF)
svenska (SV) (518.2 KB - PDF)
Nobivac Piro : EPAR - All Authorised presentations
English (EN) (478.57 KB - PDF)
български (BG) (991.68 KB - PDF)
español (ES) (480.59 KB - PDF)
čeština (CS) (522.66 KB - PDF)
dansk (DA) (478.81 KB - PDF)
Deutsch (DE) (478.47 KB - PDF)
eesti keel (ET) (496.03 KB - PDF)
ελληνικά (EL) (523.08 KB - PDF)
français (FR) (482.25 KB - PDF)
italiano (IT) (477.91 KB - PDF)
latviešu valoda (LV) (528.69 KB - PDF)
lietuvių kalba (LT) (522.74 KB - PDF)
magyar (HU) (509.76 KB - PDF)
Malti (MT) (524.91 KB - PDF)
Nederlands (NL) (479.22 KB - PDF)
polski (PL) (527.01 KB - PDF)
português (PT) (479.46 KB - PDF)
română (RO) (525.68 KB - PDF)
slovenčina (SK) (520.58 KB - PDF)
slovenščina (SL) (495.59 KB - PDF)
Suomi (FI) (476.53 KB - PDF)
svenska (SV) (479.54 KB - PDF)
Product details
- Name of medicine
- Nobivac Piro
- Active substance
- babesia canis, inactivated
- babesia rossi, inactivated
- International non-proprietary name (INN) or common name
- vaccine against babesiosis in dogs
- Species
- Dogs
- Anatomical therapeutic chemical veterinary (ATCvet) code
- QI07AO
Pharmacotherapeutic group
Immunologicals for canidaeTherapeutic indication
For active immunisation of dogs of six months of age or older against Babesia canis to reduce the severity of clinical signs associated with acute babesiosis (B. canis) and anaemia as measured by packed cell volume.
Onset of immunity: Three weeks after the basic vaccination course.
Duration of immunity: Six months after the last (re-)vaccination.
Authorisation details
- EMA product number
- EMEA/V/C/000084
- Marketing authorisation holder
- Intervet International BV
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands - Marketing authorisation issued
- 02/09/2004
- Revision
- 4
Assessment history
Nobivac Piro : EPAR - Procedural steps taken and scientific information after authorisation
English (EN) (482.7 KB - PDF)