Activyl Tick Plus

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Withdrawn

This medicine's authorisation has been withdrawn

indoxacarb / permethrin
MedicineVeterinaryWithdrawn
  • Application under evaluation
  • CVMP opinion
  • European Commission decision

Overview

The marketing authorisation for this product has been withdrawn at the request of the marketing authorisation holder.

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Product information

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íslenska (IS) (1.19 MB - PDF)

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italiano (IT) (1.04 MB - PDF)

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latviešu valoda (LV) (1.51 MB - PDF)

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lietuvių kalba (LT) (1.15 MB - PDF)

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magyar (HU) (2.01 MB - PDF)

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Latest procedure affecting product information: IB/0016
29/09/2022

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español (ES) (627.24 KB - PDF)

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čeština (CS) (635.54 KB - PDF)

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dansk (DA) (603.91 KB - PDF)

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Deutsch (DE) (607.63 KB - PDF)

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eesti keel (ET) (601.07 KB - PDF)

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ελληνικά (EL) (1.3 MB - PDF)

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français (FR) (615.71 KB - PDF)

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italiano (IT) (601.55 KB - PDF)

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latviešu valoda (LV) (676.21 KB - PDF)

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lietuvių kalba (LT) (606.83 KB - PDF)

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magyar (HU) (636.93 KB - PDF)

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Malti (MT) (640.99 KB - PDF)

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Nederlands (NL) (602.69 KB - PDF)

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polski (PL) (666.18 KB - PDF)

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português (PT) (608.07 KB - PDF)

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română (RO) (603.15 KB - PDF)

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slovenčina (SK) (636.61 KB - PDF)

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slovenščina (SL) (634.11 KB - PDF)

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Suomi (FI) (600.94 KB - PDF)

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svenska (SV) (603.5 KB - PDF)

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Product details

Name of medicine
Activyl Tick Plus
Active substance
  • indoxacarb
  • permethrin
International non-proprietary name (INN) or common name
  • indoxacarb
  • permethrin
Species
Dogs
Anatomical therapeutic chemical veterinary (ATCvet) code
QP53AC54

Pharmacotherapeutic group

  • permethrin, combinations
  • Ectoparasiticides for topical use, incl. insecticides

Therapeutic indication

Treatment of flea infestations (Ctenocephalides felis); the product has persistent insecticidal efficacy for up to 4 weeks against Ctenocephalides felis. The product has persistent acaricidal efficacy for up to 5 weeks against Ixodes ricinus and up to 3 weeks against Rhipicephalus sanguineus. One treatment provides repellent (anti-feeding) activity against sand flies (Phlebotomus perniciosus) for up to 3 weeks.

Authorisation details

EMA product number
EMEA/V/C/002234
Marketing authorisation holder
Intervet International BV

Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Opinion adopted
10/11/2011
Marketing authorisation issued
09/01/2012
Revision
9

Assessment history

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