Nobivac Piro

RSS

Withdrawn

This medicine's authorisation has been withdrawn

vaccine against babesiosis in dogs
MedicineVeterinaryWithdrawn

Italian is available via eTranslation, the European Commission's machine translation service.

Translate to Italian | Important information about machine translation

  • 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The marketing authorisation for Nobivac Piro has been withdrawn at the request of the marketing-authorisation holder.

български (BG) (623.96 KB - PDF)

Visualizza

español (ES) (517.22 KB - PDF)

Visualizza

čeština (CS) (603.97 KB - PDF)

Visualizza

dansk (DA) (513.68 KB - PDF)

Visualizza

Deutsch (DE) (520.41 KB - PDF)

Visualizza

eesti (ET) (512.62 KB - PDF)

Visualizza

ελληνικά (EL) (627.36 KB - PDF)

Visualizza

français (FR) (513.51 KB - PDF)

Visualizza

italiano (IT) (515.38 KB - PDF)

Visualizza

latviešu (LV) (599.43 KB - PDF)

Visualizza

lietuvių (LT) (598.49 KB - PDF)

Visualizza

magyar (HU) (595.88 KB - PDF)

Visualizza

Malti (MT) (620.17 KB - PDF)

Visualizza

Nederlands (NL) (514.6 KB - PDF)

Visualizza

polski (PL) (613.03 KB - PDF)

Visualizza

português (PT) (515.53 KB - PDF)

Visualizza

română (RO) (596.07 KB - PDF)

Visualizza

slovenčina (SK) (602.34 KB - PDF)

Visualizza

slovenščina (SL) (585.83 KB - PDF)

Visualizza

suomi (FI) (514.11 KB - PDF)

Visualizza

svenska (SV) (513.89 KB - PDF)

Visualizza

Product information

български (BG) (618.96 KB - PDF)

Visualizza

español (ES) (518.88 KB - PDF)

Visualizza

čeština (CS) (624.87 KB - PDF)

Visualizza

dansk (DA) (515.6 KB - PDF)

Visualizza

Deutsch (DE) (519.99 KB - PDF)

Visualizza

eesti (ET) (531.06 KB - PDF)

Visualizza

ελληνικά (EL) (618.69 KB - PDF)

Visualizza

français (FR) (513.56 KB - PDF)

Visualizza

italiano (IT) (538.08 KB - PDF)

Visualizza

latviešu (LV) (603.69 KB - PDF)

Visualizza

lietuvių (LT) (602.15 KB - PDF)

Visualizza

magyar (HU) (590.63 KB - PDF)

Visualizza

Malti (MT) (610.8 KB - PDF)

Visualizza

Nederlands (NL) (532.11 KB - PDF)

Visualizza

polski (PL) (634.94 KB - PDF)

Visualizza

português (PT) (535.76 KB - PDF)

Visualizza

română (RO) (609.2 KB - PDF)

Visualizza

slovenčina (SK) (628.87 KB - PDF)

Visualizza

slovenščina (SL) (587.55 KB - PDF)

Visualizza

suomi (FI) (514.44 KB - PDF)

Visualizza

svenska (SV) (518.2 KB - PDF)

Visualizza
Latest procedure affecting product information:R/0006
22/05/2013

български (BG) (991.68 KB - PDF)

Visualizza

español (ES) (480.59 KB - PDF)

Visualizza

čeština (CS) (522.66 KB - PDF)

Visualizza

dansk (DA) (478.81 KB - PDF)

Visualizza

Deutsch (DE) (478.47 KB - PDF)

Visualizza

eesti (ET) (496.03 KB - PDF)

Visualizza

ελληνικά (EL) (523.08 KB - PDF)

Visualizza

français (FR) (482.25 KB - PDF)

Visualizza

italiano (IT) (477.91 KB - PDF)

Visualizza

latviešu (LV) (528.69 KB - PDF)

Visualizza

lietuvių (LT) (522.74 KB - PDF)

Visualizza

magyar (HU) (509.76 KB - PDF)

Visualizza

Malti (MT) (524.91 KB - PDF)

Visualizza

Nederlands (NL) (479.22 KB - PDF)

Visualizza

polski (PL) (527.01 KB - PDF)

Visualizza

português (PT) (479.46 KB - PDF)

Visualizza

română (RO) (525.68 KB - PDF)

Visualizza

slovenčina (SK) (520.58 KB - PDF)

Visualizza

slovenščina (SL) (495.59 KB - PDF)

Visualizza

suomi (FI) (476.53 KB - PDF)

Visualizza

svenska (SV) (479.54 KB - PDF)

Visualizza

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 canidae

Therapeutic 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

This page was last updated on

Share this page