Sprimeo HCT

RSS

Withdrawn

This medicine's authorisation has been withdrawn

aliskiren / hydrochlorothiazide
MedicineHumanWithdrawn

Swedish is available via eTranslation, the European Commission's machine translation service.

Translate to Swedish | Important information about machine translation

  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 23 June 2011 the European Commission issued a marketing authorisation valid throughout the European Union for the medicinal product Sprimeo HCT (aliskiren/hydrochlorothiazide). Sprimeo HCT was approved for the treatment of essential hypertension. The marketing authorisation holder (MAH) responsible for Sprimeo HCT was Novartis Europharm Ltd. 

The European Commission was notified by letter dated 10 June 2012 of the MAH’s decision to voluntarily withdraw the marketing authorisation for Sprimeo HCT for commercial reasons. On 6 July 2012 the European Commission issued a decision to withdraw the marketing authorisation for Sprimeo HCT. 

Pursuant to this decision the European Public Assessment Report for Sprimeo HCT is updated to reflect the fact that the marketing authorisation is no longer valid.

български (BG) (344.22 KB - PDF)

Visa

español (ES) (275.46 KB - PDF)

Visa

čeština (CS) (312.8 KB - PDF)

Visa

dansk (DA) (260.03 KB - PDF)

Visa

Deutsch (DE) (320.54 KB - PDF)

Visa

eesti (ET) (258.94 KB - PDF)

Visa

ελληνικά (EL) (349.3 KB - PDF)

Visa

français (FR) (336.49 KB - PDF)

Visa

italiano (IT) (276.46 KB - PDF)

Visa

latviešu (LV) (316.91 KB - PDF)

Visa

lietuvių (LT) (284.77 KB - PDF)

Visa

magyar (HU) (369.41 KB - PDF)

Visa

Malti (MT) (313.89 KB - PDF)

Visa

Nederlands (NL) (319.44 KB - PDF)

Visa

polski (PL) (372.58 KB - PDF)

Visa

português (PT) (319.17 KB - PDF)

Visa

română (RO) (283.97 KB - PDF)

Visa

slovenčina (SK) (312.2 KB - PDF)

Visa

slovenščina (SL) (308.57 KB - PDF)

Visa

suomi (FI) (320.75 KB - PDF)

Visa

svenska (SV) (319.66 KB - PDF)

Visa

Product information

български (BG) (4.72 MB - PDF)

Visa

español (ES) (1.87 MB - PDF)

Visa

čeština (CS) (3.27 MB - PDF)

Visa

dansk (DA) (1.89 MB - PDF)

Visa

Deutsch (DE) (1.91 MB - PDF)

Visa

eesti (ET) (2.1 MB - PDF)

Visa

ελληνικά (EL) (4.89 MB - PDF)

Visa

français (FR) (2.22 MB - PDF)

Visa

italiano (IT) (1.94 MB - PDF)

Visa

latviešu (LV) (3.49 MB - PDF)

Visa

lietuvių (LT) (2.06 MB - PDF)

Visa

magyar (HU) (3.36 MB - PDF)

Visa

Malti (MT) (3.66 MB - PDF)

Visa

Nederlands (NL) (1.95 MB - PDF)

Visa

polski (PL) (3.61 MB - PDF)

Visa

português (PT) (1.88 MB - PDF)

Visa

română (RO) (2.05 MB - PDF)

Visa

slovenčina (SK) (3.44 MB - PDF)

Visa

slovenščina (SL) (3.4 MB - PDF)

Visa

suomi (FI) (1.86 MB - PDF)

Visa

svenska (SV) (1.85 MB - PDF)

Visa

Íslenska (IS) (2.06 MB - PDF)

Visa

norsk (NO) (2.01 MB - PDF)

Visa
Latest procedure affecting product information:-
06/07/2012
icon globe

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) (544.13 KB - PDF)

Visa

español (ES) (455.93 KB - PDF)

Visa

čeština (CS) (481.57 KB - PDF)

Visa

dansk (DA) (451.09 KB - PDF)

Visa

Deutsch (DE) (460.1 KB - PDF)

Visa

eesti (ET) (456.43 KB - PDF)

Visa

ελληνικά (EL) (565.21 KB - PDF)

Visa

français (FR) (462.9 KB - PDF)

Visa

italiano (IT) (455.29 KB - PDF)

Visa

latviešu (LV) (488.67 KB - PDF)

Visa

lietuvių (LT) (466.48 KB - PDF)

Visa

magyar (HU) (514.93 KB - PDF)

Visa

Malti (MT) (488.16 KB - PDF)

Visa

Nederlands (NL) (456.23 KB - PDF)

Visa

polski (PL) (484.36 KB - PDF)

Visa

português (PT) (455.22 KB - PDF)

Visa

română (RO) (464.08 KB - PDF)

Visa

slovenčina (SK) (483.52 KB - PDF)

Visa

slovenščina (SL) (494.28 KB - PDF)

Visa

suomi (FI) (457.04 KB - PDF)

Visa

svenska (SV) (454.24 KB - PDF)

Visa

Íslenska (IS) (455.05 KB - PDF)

Visa

norsk (NO) (456.64 KB - PDF)

Visa

Product details

Name of medicine
Sprimeo HCT
Active substance
  • aliskiren
  • hydrochlorothiazide
International non-proprietary name (INN) or common name
  • aliskiren
  • hydrochlorothiazide
Therapeutic area (MeSH)
Hypertension
Anatomical therapeutic chemical (ATC) code
C09XA52

Pharmacotherapeutic group

Agents acting on the renin-angiotensin system

Therapeutic indication

Treatment of essential hypertension in adults.

Sprimeo HCT is indicated in patients whose blood pressure is not adequately controlled on aliskiren or hydrochlorothiazide used alone.

Sprimeo HCT is indicated as substitution therapy in patients adequately controlled with aliskiren and hydrochlorothiazide, given concurrently, at the same dose level as in the combination.

Authorisation details

EMA product number
EMEA/H/C/002421
Marketing authorisation holder
Novartis Europharm Ltd.

Wimblehurst Road
Horsham
West Sussex
RH12 5AB
United Kingdom

Marketing authorisation issued
23/06/2011
Withdrawal of marketing authorisation
06/07/2012

Assessment history

This page was last updated on

Share this page