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Razadyne

Galantamine · also sold as Razadyne / Reminyl

An oral daily medication used to treat mild to moderate dementia in Alzheimer's disease.

Generic name
Galantamine
Brand names
Razadyne / Reminyl
Marketed by
Janssen (Johnson & Johnson)
First FDA approval
28 Feb 2001

Where Galantamine is approved

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Of the three regulators tracked here, the first to approve Galantamine was the US, on 28 Feb 2001. It is approved in 2 of the 3 regulators tracked here.

USUnited States (FDA)
28 Feb 2001
Razadyne
NDA021169 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
31 Jul 2001
Reminyl
Notice of Compliance 2292
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

What health systems spend on Galantamine

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ENNHS England
£5.7m
97,763 items dispensed, Aug 2025 to Jul 2026
+8% on the previous 12 months
Net ingredient cost, community prescriptions
USUS Medicaid
$240k
7,060 prescriptions in 2025 · Galantamine, Galantamine Hydrobromide
-2% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

How Galantamine works

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  • Acetylcholinesterase inhibitor Inhibitor
    Target: ACHE acetylcholinesterase (Yt blood group)
    ✓ In ChEMBL and the Guide to Pharmacology
Other medicines acting on ACHE
Diseases it has been tested for in clinical trials, by furthest phase
  • Lewy body dementiaPhase 3
  • AutismPhase 3
  • Vascular dementiaPhase 3
  • Ischemic strokePhase 2/3
  • SchizophreniaPhase 2/3
  • Cognitive impairmentPhase 2
  • HIV infectious diseasePhase 2
  • HIV-associated neurocognitive disorderPhase 2
  • Cocaine dependencePhase 2
  • Cocaine use disorderPhase 2
21 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL659, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3), ligand 6693, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

NICE appraisals of Galantamine

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NICE, which decides whether the NHS in England should fund new medicines, has published 3 technology appraisals of Galantamine. 2 are current, and 2 of these recommend it for at least some patients. 1 older appraisal was replaced or withdrawn.

AppraisalNICE recommendationPublishedStatus
Donepezil, galantamine, rivastigmine and memantine for the treatment of Alzheimer's disease
NICE TA217
Recommended Optimised23 Mar 2011
Updated 20 Jun 2018
Current
Donepezil, galantamine, rivastigmine and memantine for the treatment of Alzheimer's disease
NICE TA111
Optimised Only in research22 Nov 2006Current

NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.

Patient leaflets for Galantamine

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Galantamine

ATC code
N06DA04
ChEMBL
CHEMBL659
DrugBank
DB00674
PubChem CID
9651
CAS number
357-70-0
FDA UNII
1T835Z585R
Wikidata
Q412690
Wikipedia
Galantamine

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

What Razadyne is used for

Galantamine (Razadyne / Reminyl) is an oral daily medication used to treat mild to moderate dementia in Alzheimer's disease. It belongs to the Cholinesterase inhibitor class.

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How this page is built

The facts on this page are pulled directly from official U.S. FDA datasets — they are not written from memory. Each field below names the dataset it came from, so you can check it yourself.

Plain-English summaries and drug-class explainers are written and reviewed by Sreepriya Prasannan (MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany). Data is retrieved automatically from the sources above and cross-checked with AI-assisted verification (Anthropic's Claude) — brand and generic names are matched against the exact FDA product record so that a combination product or a different formulation cannot be mistaken for the drug on this page. An editor reviews the result before publication. We describe this in full in our editorial standards and corrections policy. The FDA data on this page was last retrieved on 11 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.