Episalvan

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Withdrawn

This medicine's authorisation has been withdrawn

birch bark extract
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 7 June 2022, the European Commission withdrew the marketing authorisation for Episalvan (birch bark extract) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Amryt GmbH, which notified the European Commission of its decision not to market the product in the EU for commercial reasons. 

Episalvan was granted marketing authorisation in the EU on 14 January 2016 for the treatment of partial thickness wounds in adults. 

The European Public Assessment Report (EPAR) for Episalvan is updated to indicate that the marketing authorisation is no longer valid.

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Product information

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dansk (DA) (413.47 KB - PDF)

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Deutsch (DE) (432.51 KB - PDF)

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eesti (ET) (398.81 KB - PDF)

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ελληνικά (EL) (843.43 KB - PDF)

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français (FR) (426.81 KB - PDF)

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hrvatski (HR) (494.83 KB - PDF)

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italiano (IT) (413.48 KB - PDF)

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latviešu (LV) (676.12 KB - PDF)

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lietuvių (LT) (503.12 KB - PDF)

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magyar (HU) (653.64 KB - PDF)

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Malti (MT) (668.13 KB - PDF)

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Nederlands (NL) (420.11 KB - PDF)

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polski (PL) (672.77 KB - PDF)

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português (PT) (413.49 KB - PDF)

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română (RO) (513.12 KB - PDF)

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slovenčina (SK) (659.65 KB - PDF)

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slovenščina (SL) (633.51 KB - PDF)

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suomi (FI) (464.57 KB - PDF)

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svenska (SV) (412.87 KB - PDF)

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Íslenska (IS) (412.08 KB - PDF)

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norsk (NO) (409.62 KB - PDF)

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07/06/2022
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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

български (BG) (213.15 KB - PDF)

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español (ES) (179.64 KB - PDF)

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čeština (CS) (206.85 KB - PDF)

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dansk (DA) (178.94 KB - PDF)

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Deutsch (DE) (179.35 KB - PDF)

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eesti (ET) (179.37 KB - PDF)

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ελληνικά (EL) (214.3 KB - PDF)

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français (FR) (178.46 KB - PDF)

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hrvatski (HR) (192.58 KB - PDF)

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italiano (IT) (180 KB - PDF)

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latviešu (LV) (238.07 KB - PDF)

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lietuvių (LT) (197.73 KB - PDF)

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magyar (HU) (204.56 KB - PDF)

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Malti (MT) (207.5 KB - PDF)

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Nederlands (NL) (179.14 KB - PDF)

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polski (PL) (206.18 KB - PDF)

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português (PT) (179.38 KB - PDF)

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română (RO) (196.46 KB - PDF)

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slovenčina (SK) (206.29 KB - PDF)

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slovenščina (SL) (200.6 KB - PDF)

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suomi (FI) (180.06 KB - PDF)

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svenska (SV) (180.74 KB - PDF)

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Íslenska (IS) (184.82 KB - PDF)

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norsk (NO) (184.87 KB - PDF)

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Product details

Name of medicine
Episalvan
Active substance
Betulae cortex
International non-proprietary name (INN) or common name
birch bark extract
Therapeutic area (MeSH)
  • Wounds and Injuries
  • Wound Healing
Anatomical therapeutic chemical (ATC) code
D03AX13

Pharmacotherapeutic group

Preparations for treatment of wounds and ulcers

Therapeutic indication

Treatment of partial thickness wounds in adults. See sections 4.4 and 5.1 in Product Information with respect to type of wounds studied.

Authorisation details

EMA product number
EMEA/H/C/003938
Marketing authorisation holder
Amryt AG

Streiflingsweg 11
75223 Niefern-Oschelbronn
Germany

Opinion adopted
19/11/2015
Marketing authorisation issued
14/01/2016
Withdrawal of marketing authorisation
07/06/2022
Revision
7

Assessment history

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