Nobivac Piro

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Withdrawn

This medicine's authorisation has been withdrawn

vaccine against babesiosis in dogs
MedicineVeterinaryWithdrawn

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The marketing authorisation for Nobivac Piro has been withdrawn at the request of the marketing-authorisation holder.

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Product information

български (BG) (618.96 KB - PDF)

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español (ES) (518.88 KB - PDF)

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čeština (CS) (624.87 KB - PDF)

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italiano (IT) (538.08 KB - PDF)

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latviešu (LV) (603.69 KB - PDF)

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magyar (HU) (590.63 KB - PDF)

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

български (BG) (991.68 KB - PDF)

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español (ES) (480.59 KB - PDF)

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čeština (CS) (522.66 KB - PDF)

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dansk (DA) (478.81 KB - PDF)

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Deutsch (DE) (478.47 KB - PDF)

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eesti (ET) (496.03 KB - PDF)

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ελληνικά (EL) (523.08 KB - PDF)

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français (FR) (482.25 KB - PDF)

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italiano (IT) (477.91 KB - PDF)

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latviešu (LV) (528.69 KB - PDF)

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lietuvių (LT) (522.74 KB - PDF)

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magyar (HU) (509.76 KB - PDF)

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Malti (MT) (524.91 KB - PDF)

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Nederlands (NL) (479.22 KB - PDF)

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polski (PL) (527.01 KB - PDF)

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português (PT) (479.46 KB - PDF)

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română (RO) (525.68 KB - PDF)

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slovenčina (SK) (520.58 KB - PDF)

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slovenščina (SL) (495.59 KB - PDF)

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suomi (FI) (476.53 KB - PDF)

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svenska (SV) (479.54 KB - PDF)

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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

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