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Two medicines, side by side

Eletriptan vs rizatriptan

Eletriptan and rizatriptan are both labeled for migraine. Drugs@FDA records approvals of eletriptan since 2002 and of rizatriptan since 1998. Pharmacies paid $1.75 per eletriptan hbr 40 mg tablet and $0.335 per rizatriptan 10 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Eletriptan, “Eletriptan binds with high affinity to 5-HT 1B , 5-HT 1D and 5-HT 1F receptors, has modest affinity for 5-HT 1A , 5-HT 1E , 5-HT 2B and 5-HT 7 receptors.”; Rizatriptan, “Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.”

Check it at the source: the eletriptan FDA label on DailyMed (effective November 27, 2024); the rizatriptan FDA label on DailyMed (effective January 29, 2026).

Highlights of the eletriptan record

Eletriptan (Relpax) · label of November 27, 2024

Used for

From the label: indications

Eletriptan hydrobromide tablets are indicated for the acute treatment of migraine with or without aura in adults. Limitations of Use: Use only if a clear diagnosis of migraine has been established. […]

On the market

Earliest approval on file
December 26, 2002
Generic labelers
10 labelers
Pharmacy cost
$1.75 per tablet

Supply and safety

Shortage
No current entry
Recalls
1

Highlights of the rizatriptan record

Rizatriptan (Maxalt) · label of January 29, 2026

Used for

From the label: indications

MAXALT ® and MAXALT-MLT ® are indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years old. Limitations of Use MAXALT should only be used where a clear diagnosis of migraine has been established. […]

On the market

Earliest approval on file
June 29, 1998
Generic labelers
22 labelers
Pharmacy cost
$0.335 per tablet

Supply and safety

Shortage
No current entry
Recalls
9

Source: FDA drug labels via openFDA (Eletriptan label of November 27, 2024, Rizatriptan label of January 29, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do eletriptan and rizatriptan differ on the record?

How each works, in its label's words: Eletriptan, “Eletriptan binds with high affinity to 5-HT 1B , 5-HT 1D and 5-HT 1F receptors, has modest affinity for 5-HT 1A , 5-HT 1E , 5-HT 2B and 5-HT 7 receptors.”; Rizatriptan, “Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.”

Both are in FDA's class serotonin-1b and serotonin-1d receptor agonists.

Half-life, in each label's words: Eletriptan, “Elimination: The terminal elimination half-life of eletriptan is approximately 4 hours.”; Rizatriptan, “The plasma half-life of rizatriptan in males and females averages 2-3 hours.”

Generics: eletriptan since 2017; rizatriptan since 2012 (Drugs@FDA).

EletriptanRizatriptan
Labeled forMigraineMigraine
Pharmacologic classSerotonin-1b and Serotonin-1d Receptor AgonistSerotonin-1b and Serotonin-1d Receptor Agonist
How it works (label)Eletriptan binds with high affinity to 5-HT 1B , 5-HT 1D and 5-HT 1F receptors, has modest affinity for 5-HT 1A , 5-HT 1E , 5-HT 2B and 5-HT 7 receptors.Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.
Half-life (label)Elimination: The terminal elimination half-life of eletriptan is approximately 4 hours.The plasma half-life of rizatriptan in males and females averages 2-3 hours.
Earliest approval on file (Drugs@FDA)December 26, 2002June 29, 1998
First generic approvedJune 16, 2017December 31, 2012
Generic labelers (NDC)10 labelers22 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$1.75 per tablet (Eletriptan hbr 40 mg tablet)$0.335 per tablet (Rizatriptan 10 mg tablet)
12-month price change-15%-34%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded19
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)6,99616,132
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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