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Two medicines, side by side

Rivastigmine vs memantine

Rivastigmine and memantine are both labeled for alzheimer's disease. Drugs@FDA records approvals of rivastigmine since 2000 and of memantine since 2003. Pharmacies paid $0.164 per rivastigmine 1.5 mg capsule and $0.063 per memantine HCl 10 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, rivastigmine is a cholinesterase inhibitor and memantine a n-methyl-d-aspartate receptor antagonist.

Check it at the source: the rivastigmine FDA label on DailyMed (effective June 19, 2024); the memantine FDA label on DailyMed (effective November 1, 2018).

Highlights of the rivastigmine record

Rivastigmine (Exelon) · label of June 19, 2024

Used for

From the label: indications

Rivastigmine tartrate capsules are an acetylcholinesterase inhibitor indicated for treatment of: Mild-to-moderate dementia of the Alzheimer’s type (AD) ( 1.1 ) Mild-to-moderate dementia associated with Parkinson’s disease (PD) ( 1.2 ) 1.1 Alzheimer’s Disease Rivastigmine tartrate capsules are indicated for the treatment of mild-to-moderate dementia of the Alzheimer's type (AD). 1.2 Parkinson’s Disease Dementia Rivastigmine tartrate capsules are indicated for the treatment of mild-to-moderate dementia associated with Parkinson’s disease (PD). […]

On the market

Earliest approval on file
April 21, 2000
Generic labelers
18 labelers
Pharmacy cost
$0.164 per capsule

Supply and safety

Shortage
A presentation being discontinued
Recalls
2

Highlights of the memantine record

Memantine (Namenda) · label of November 1, 2018

Used for

From the label: indications

Memantine hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride tablets are an N-methyl-D-aspartate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer’s type.

On the market

Earliest approval on file
October 16, 2003
Generic labelers
38 labelers
Pharmacy cost
$0.063 per tablet

Supply and safety

Shortage
No current entry
Recalls
7

Source: FDA drug labels via openFDA (Rivastigmine label of June 19, 2024, Memantine label of November 1, 2018); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do rivastigmine and memantine differ on the record?

In FDA's classes, rivastigmine is a cholinesterase inhibitor and memantine a n-methyl-d-aspartate receptor antagonist.

How each works, in its label's words: Rivastigmine, “Although the precise mechanism of action of rivastigmine is unknown, it is thought to exert its therapeutic effect by enhancing cholinergic function.”; Memantine, “Persistent activation of central nervous system N-methyl-D-aspartate (NMDA) receptors by the excitatory amino acid glutamate has been hypothesized to contribute to the symptomatology of Alzheimer’s …”

Generics: rivastigmine since 2007; memantine since 2010 (Drugs@FDA).

RivastigmineMemantine
Labeled forAlzheimer's diseaseAlzheimer's disease
Pharmacologic classCholinesterase InhibitorN-methyl-D-aspartate Receptor Antagonist
How it works (label)Although the precise mechanism of action of rivastigmine is unknown, it is thought to exert its therapeutic effect by enhancing cholinergic function.Persistent activation of central nervous system N-methyl-D-aspartate (NMDA) receptors by the excitatory amino acid glutamate has been hypothesized to contribute to the symptomatology of Alzheimer’s disease.
Half-life (label)The elimination half-life is about 1.5 hours, with most elimination as metabolites via the urine.n/a
Earliest approval on file (Drugs@FDA)April 21, 2000October 16, 2003
First generic approvedOctober 22, 2007April 14, 2010
Generic labelers (NDC)18 labelers38 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.164 per capsule (Rivastigmine 1.5 mg capsule)$0.063 per tablet (Memantine HCl 10 mg tablet)
12-month price change-11%-1%
Boxed warningNoNo
Shortage nowA presentation being discontinuedNo current entry
Recalls recorded27
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)19,15913,605
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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