Pruban

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

resocortol butyrate

Available from:

Intervet International BV

ATC code:

QD07AC90

INN (International Name):

resocortol butyrate

Therapeutic group:

Klieb

Therapeutic area:

Kortikosterojdi, preparazzjonijiet dermatoloġiċi

Therapeutic indications:

Trattament ta 'dermatite umda lokalizzata akuta.

Product summary:

Revision: 4

Authorization status:

Irtirat

Authorization date:

2000-11-16

Documents in other languages

Public Assessment Report Public Assessment Report Bulgarian 26-07-2010
Patient Information leaflet Patient Information leaflet Spanish 26-07-2010
Public Assessment Report Public Assessment Report Spanish 26-07-2010
Patient Information leaflet Patient Information leaflet Czech 26-07-2010
Public Assessment Report Public Assessment Report Czech 26-07-2010
Patient Information leaflet Patient Information leaflet Danish 26-07-2010
Public Assessment Report Public Assessment Report Danish 26-07-2010
Patient Information leaflet Patient Information leaflet German 26-07-2010
Public Assessment Report Public Assessment Report German 26-07-2010
Patient Information leaflet Patient Information leaflet Estonian 26-07-2010
Public Assessment Report Public Assessment Report Estonian 26-07-2010
Patient Information leaflet Patient Information leaflet Greek 26-07-2010
Public Assessment Report Public Assessment Report Greek 26-07-2010
Patient Information leaflet Patient Information leaflet English 26-07-2010
Public Assessment Report Public Assessment Report English 26-07-2010
Patient Information leaflet Patient Information leaflet French 26-07-2010
Public Assessment Report Public Assessment Report French 26-07-2010
Patient Information leaflet Patient Information leaflet Italian 26-07-2010
Public Assessment Report Public Assessment Report Italian 26-07-2010
Patient Information leaflet Patient Information leaflet Latvian 26-07-2010
Public Assessment Report Public Assessment Report Latvian 26-07-2010
Patient Information leaflet Patient Information leaflet Lithuanian 26-07-2010
Summary of Product characteristics Summary of Product characteristics Lithuanian 26-07-2010
Public Assessment Report Public Assessment Report Lithuanian 26-07-2010
Patient Information leaflet Patient Information leaflet Hungarian 26-07-2010
Summary of Product characteristics Summary of Product characteristics Hungarian 26-07-2010
Public Assessment Report Public Assessment Report Hungarian 26-07-2010
Patient Information leaflet Patient Information leaflet Dutch 26-07-2010
Public Assessment Report Public Assessment Report Dutch 26-07-2010
Patient Information leaflet Patient Information leaflet Polish 26-07-2010
Public Assessment Report Public Assessment Report Polish 26-07-2010
Patient Information leaflet Patient Information leaflet Portuguese 26-07-2010
Summary of Product characteristics Summary of Product characteristics Portuguese 26-07-2010
Public Assessment Report Public Assessment Report Portuguese 26-07-2010
Public Assessment Report Public Assessment Report Romanian 26-07-2010
Patient Information leaflet Patient Information leaflet Slovak 26-07-2010
Public Assessment Report Public Assessment Report Slovak 26-07-2010
Patient Information leaflet Patient Information leaflet Slovenian 26-07-2010
Summary of Product characteristics Summary of Product characteristics Slovenian 26-07-2010
Public Assessment Report Public Assessment Report Slovenian 26-07-2010
Patient Information leaflet Patient Information leaflet Finnish 26-07-2010
Public Assessment Report Public Assessment Report Finnish 26-07-2010
Patient Information leaflet Patient Information leaflet Swedish 26-07-2010
Public Assessment Report Public Assessment Report Swedish 26-07-2010

Search alerts related to this product

View documents history