Imprida (amlodipine;valsartan)
- Region
- 🇪🇺 EU
- Active substance
- amlodipine;valsartan
- Company
- Novartis Europharm Ltd
- Status
- Withdrawn
- Therapeutic area
- Hypertension
- EU approval
- Wed 17 Jan 2007
- Application
- EMEA/H/C/000775
- ATC
- C09DB01
- Official record
- www.ema.europa.eu
Indication
Treatment of essential hypertension. Imprida is indicated in patients whose blood pressure is not adequately controlled on amlodipine or valsartan monotherapy.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Amlodipine / Valsartan Mylan Authorised · Mylan Pharmaceuticals Limited
- 🇪🇺 Copalia HCT Authorised · Novartis Europharm Limited
- 🇪🇺 Copalia Authorised · Novartis Europharm Limited
- 🇪🇺 Dafiro Authorised · Novartis Europharm Limited
- 🇪🇺 Exforge Authorised · Novartis Europharm Limited
- 🇪🇺 Imprida HCT Lapsed · Novartis Europharm Ltd.
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.