Pruban

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Withdrawn

This medicine's authorisation has been withdrawn

resocortol butyrate
MedicineVeterinaryWithdrawn
  • Application under evaluation
  • CVMP opinion
  • European Commission decision

Overview

The marketing authorisation for Pruban has not been renewed by the marketing authorisation holder and is now withdrawn.

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Product information

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lietuvių kalba (LT) (383.77 KB - PDF)

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polski (PL) (433.61 KB - PDF)

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português (PT) (278.3 KB - PDF)

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slovenčina (SK) (407.07 KB - PDF)

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slovenščina (SL) (390.53 KB - PDF)

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Suomi (FI) (280.98 KB - PDF)

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svenska (SV) (281.17 KB - PDF)

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Latest procedure affecting product information: R/0004
14/06/2010

Product details

Name of medicine
Pruban
Active substance
resocortol butyrate
International non-proprietary name (INN) or common name
resocortol butyrate
Species
Dogs
Anatomical therapeutic chemical veterinary (ATCvet) code
QD07AC90

Pharmacotherapeutic group

Corticosteroids, dermatological preparations

Therapeutic indication

Treatment of acute localised moist dermatitis.

Authorisation details

EMA product number
EMEA/V/C/000048
Marketing authorisation holder
Intervet International BV

Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Marketing authorisation issued
16/11/2000
Revision
4

Assessment history

This page was last updated on

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