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Two medicines, side by side

Rizatriptan vs sumatriptan

Rizatriptan and sumatriptan are both labeled for migraine. Drugs@FDA records approvals of rizatriptan since 1998 and of sumatriptan since 1992. Pharmacies paid $0.335 per rizatriptan 10 mg tablet and $0.302 per sumatriptan succ 50 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Sumatriptan's other strengths are brand-only: $108.22 per unit (Tosymra 10 mg nasal spray). How each works, in its label's words: Rizatriptan, “Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.”; Sumatriptan, “Sumatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.”

Check it at the source: the rizatriptan FDA label on DailyMed (effective January 29, 2026); the sumatriptan FDA label on DailyMed (effective May 12, 2026).

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

Highlights of the sumatriptan record

Sumatriptan (Imitrex) · label of May 12, 2026

Used for

From the label: indications

Sumatriptan 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 headache has been established. If a patient has no response to the first migraine attack treated with sumatriptan tablets, reconsider the diagnosis of migraine before sumatriptan tablets are administered to treat any subsequent attacks. […]

On the market

Earliest approval on file
December 28, 1992
Generic labelers
39 labelers
Pharmacy cost
$0.302 per tablet

Supply and safety

Shortage
No current entry
Recalls
6

Source: FDA drug labels via openFDA (Rizatriptan label of January 29, 2026, Sumatriptan label of May 12, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do rizatriptan and sumatriptan differ on the record?

How each works, in its label's words: Rizatriptan, “Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.”; Sumatriptan, “Sumatriptan 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: Rizatriptan, “The plasma half-life of rizatriptan in males and females averages 2-3 hours.”; Sumatriptan, “Elimination The elimination half-life of sumatriptan is approximately 2.5 hours.”

Generics: rizatriptan since 2012; sumatriptan since 2009 (Drugs@FDA).

RizatriptanSumatriptan
Labeled forMigraineMigraine
Pharmacologic classSerotonin-1b and Serotonin-1d Receptor AgonistSerotonin-1b and Serotonin-1d Receptor Agonist
How it works (label)Rizatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.Sumatriptan binds with high affinity to human cloned 5-HT 1B/1D receptors.
Half-life (label)The plasma half-life of rizatriptan in males and females averages 2-3 hours.Elimination The elimination half-life of sumatriptan is approximately 2.5 hours.
Earliest approval on file (Drugs@FDA)June 29, 1998December 28, 1992
First generic approvedDecember 31, 2012February 6, 2009
Generic labelers (NDC)22 labelers39 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.335 per tablet (Rizatriptan 10 mg tablet)$0.302 per tablet (Sumatriptan succ 50 mg tablet)
12-month price change-34%-10%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded96
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)16,13244,847
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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