Exelon (rivastigmine)
- Region
- 🇪🇺 EU
- Active substance
- rivastigmine
- Company
- Novartis Europharm Limited
- Status
- Authorised
- Therapeutic area
- Dementia; Alzheimer Disease; Parkinson Disease
- CHMP opinion
- Wed 28 Jan 1998
- EU approval
- Mon 11 May 1998
- Application
- EMEA/H/C/000169
- ATC
- N06DA03
- Official record
- www.ema.europa.eu
Indication
Symptomatic treatment of mild to moderately severe Alzheimer's dementia. Symptomatic treatment of mild to moderately severe dementia in patients with idiopathic Parkinson's disease.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Rivastigmine Hexal Authorised · Hexal AG
- 🇪🇺 Rivastigmine Sandoz Authorised · Sandoz GmbH
- 🇪🇺 Rivastigmine 1 A Pharma Authorised · 1 A Pharma GmbH
- 🇪🇺 Nimvastid Authorised · KRKA tovarna zdravil d.d. Novo mesto
- 🇪🇺 Rivastigmine Actavis Authorised · Actavis Group PTC ehf
- 🇪🇺 Prometax Authorised · Almirall, S.A.
- 🇪🇺 Rivastigmine 3M Health Care Ltd Withdrawn · 3M Health Care Limited
- 🇪🇺 Rivastigmine Teva Withdrawn · Teva Pharma B.V.
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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.