Sumatriptan
Sumatriptan is a triptan medication used to treat acute migraine attacks across several forms and brands, and the subcutaneous injection is also approved to treat cluster headache in adults.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 57 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Sumatriptan, a triptan, is a usual first choice for stopping a migraine attack once it starts (some injection forms also treat cluster headache), working by narrowing blood vessels in the head and blocking pain chemicals released by the trigeminal nerve; it has been around since the 1990s and is available as a generic. Most people handle it well, though brief tingling, warmth, flushing or chest or neck heaviness soon after a dose is common. It narrows blood vessels elsewhere too, so it is not for people with heart disease, a past stroke or uncontrolled high blood pressure, and severe or lingering chest, jaw or throat pressure needs prompt care.
Clinical pearls
- Take it at the first sign of migraine pain; a repeat dose later only makes sense if the first one helped.
- Never use it within 24 hours of another triptan or an ergot drug such as dihydroergotamine.
- If you take an SSRI, SNRI or other antidepressant, make sure your prescriber knows, because the combination can raise serotonin syndrome risk.
- Needing it on many days each month can cause rebound headaches, so more frequent attacks call for a preventive plan.
Patient information guide A plain-language walkthrough of Sumatriptan, written from its FDA label.
What Sumatriptan is used for
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Sumatriptan is a triptan used to treat acute migraine and, with certain injection products, cluster headache attacks in adults. It is not a preventive medicine — it is taken to stop an attack that has already begun.
- Acute treatment of migraine with or without aura in adults — all forms and brands
- Acute treatment of cluster headache in adults — Imitrex injection, Sumatriptan injection, and Sumatriptan Succinate injection only
- Zembrace SymTouch (subcutaneous injection): acute migraine only; not approved for cluster headache
- Onzetra Xsail (nasal capsule), nasal sprays, and tablets: acute migraine only; not established for cluster headache
- No sumatriptan product is indicated for the prevention of migraine or cluster headache
How Sumatriptan works
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Sumatriptan binds with high affinity to serotonin receptors called 5-HT1B and 5-HT1D, found on blood vessels and sensory nerves inside the skull. Activating these receptors causes the blood vessels to constrict (narrow) and blocks the release of inflammatory chemicals from the trigeminal nerve — the nerve network at the root of migraine pain. The result is relief from the pain and other symptoms of a migraine or cluster headache attack.
Sumatriptan dosage
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Sumatriptan is available in several forms: tablets taken by mouth, nasal sprays, a breath-powered nasal capsule (Onzetra Xsail), and injections given just under the skin. The form, timing, and maximum daily amount differ by product — always follow your prescriber's instructions. Tablets can be taken with or without food, though a high-fat meal may slightly increase absorption. If a first dose helps but the headache returns, a second dose may be taken after the required waiting period, but only if the first dose gave you some relief. Do not use sumatriptan every day to prevent headaches — it is for treating attacks only, and overuse can actually worsen headaches over time.
Dosing details from the FDA-approved label
From the Sumatriptan prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Onzetra Xsail nasal powder: acute treatment of migraine
- 22 mg of sumatriptan nasal powder (2 nosepieces), one 11 mg nosepiece in each nostril
- If the migraine has not resolved by 2 hours, or returns after a transient improvement, a second dose of 22 mg may be administered at least 2 hours after the first dose
- Maximum: Two doses (44 mg/4 nosepieces) in 24 hours, separated by at least 2 hours
- Sumatriptan injection (subcutaneous): acute treatment of migraine
- Single dose of 4 mg or 6 mg injected subcutaneously
- 4 mg may be used if side effects are dose limiting
- A second 6 mg dose should only be considered if some response to a first injection was observed, separated by at least 1 hour
- Maximum: 12 mg in 24 hours (two 6 mg injections separated by at least 1 hour)
- For doses other than 6 mg, use the 6 mg single-dose vial, not the autoinjector
- Sumatriptan injection (subcutaneous): acute treatment of cluster headache
- Single dose of 6 mg injected subcutaneously
- Efficacy of lower doses has not been established
- Maximum: 12 mg in 24 hours (two 6 mg injections separated by at least 1 hour)
- Sumatriptan tablets: acute treatment of migraine in adults
- Single dose of 25 mg, 50 mg, or 100 mg
- If the migraine has not resolved by 2 hours or returns after a transient improvement, a second dose may be given at least 2 hours after the first dose
- Maximum: 200 mg in a 24-hour period
- Doses of 50 mg and 100 mg may provide a greater effect than 25 mg; higher doses may have a greater risk of adverse reactions
- Sumatriptan tablets: migraine returning after initial treatment with sumatriptan injection
- Additional single sumatriptan tablets may be given with an interval of at least 2 hours between tablet doses
- Maximum: up to 100 mg/day
- Sumatriptan tablets: patients with mild to moderate hepatic impairment
- If treatment is deemed advisable, maximum single dose should not exceed 50 mg
- Maximum: 50 mg single dose
- Hepatic impairment
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Single dose of 25 mg, 50 mg, or 100 mg tablet. ( 2.1 ) A second dose should only be considered if some response to the first dose was observed. Separate doses by at least 2 hours. ( 2.1 ) Maximum dose in a 24-hour period: 200 mg. ( 2.1 ) Maximum single dose should not exceed 50 mg in patients with mild to moderate hepatic impairment. ( 2.2 ) 2.1 Dosing Information The recommended dose of sumatriptan succinate tablets is 25 mg, 50 mg, or 100 mg. Doses of 50 mg and 100 mg may provide a greater effect than the 25 mg dose, but doses of 100 mg may not provide a greater effect than the 50 mg dose. Higher doses may have a greater risk of adverse reactions [see Clinical Studies ( 14 )]. If the migraine has not resolved by 2 hours after taking sumatriptan succinate tablets, or returns after a transient improvement, a second dose may be administered at least 2 hours after the first dose. The maximum daily dose is 200 mg in a 24-hour period. Use after sumatriptan injection If the migraine returns following an initial treatment with sumatriptan injection, additional single sumatriptan succinate tablets (up to 100 mg/day) may be given with an interval of at least 2 hours between tablet doses. The safety of treating an average of more than 4 headaches in a 30-day period has not been established. 2.2 Dosing in Patients with Hepatic Impairment If treatment is deemed advisable in the presence of mild to moderate hepatic impairment, the maximum single dose should not exceed 50 mg [see Use in Specific Populations ( 8.6 ), Clinical Pharmacology ( 12.3 )] .
Read the full Dosage and Administration section on DailyMed →
Sumatriptan side effects
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The most common side effects with sumatriptan include:
Common side effects
- Tingling or numbness
- Warm, hot, or burning sensation
- Feeling of heaviness or pressure
- Flushing
- Dizziness
- Feeling of tightness
- Injection site reactions (with the injection form)
- Nasal or throat irritation (with nasal forms)
- Nasal or throat burning, numbness, or discharge (with nasal forms)
When to get medical help
- Chest, throat, jaw, or neck pain, tightness, or pressure — get evaluated right away
- Signs of a heart attack: sudden severe chest pain, shortness of breath, sweating
- Signs of a stroke: sudden face drooping, arm weakness, speech difficulty
- Severe allergic reaction: swelling of the face or throat, hives, difficulty breathing
- Signs of serotonin syndrome: agitation, rapid heart rate, muscle twitching, fever, confusion
- Significant rise in blood pressure or symptoms of hypertensive crisis
- Seizures
- Abdominal pain or bloody diarrhea (possible bowel blood vessel spasm)
Sumatriptan warnings and precautions
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- Heart risks: Serious cardiac events including heart attack and dangerous heart rhythms have been reported, sometimes in people without known heart disease. Anyone with multiple cardiovascular risk factors needs a cardiac evaluation before starting sumatriptan.
- Stroke and cerebrovascular events: Stroke and bleeding in or around the brain have occurred with triptans. Sumatriptan is contraindicated in anyone with a history of stroke or TIA.
- Blood pressure: Significant blood pressure spikes — including hypertensive crisis — have been reported, even in people without high blood pressure. Sumatriptan is contraindicated in uncontrolled high blood pressure.
- Vasospasm elsewhere in the body: Sumatriptan can cause blood vessel spasm in the gut, limbs, or other areas, leading to symptoms like abdominal pain, bloody diarrhea, or limb coldness.
- Serotonin syndrome: A potentially dangerous buildup of serotonin activity can occur, especially when sumatriptan is combined with certain antidepressants (SSRIs, SNRIs, TCAs) or MAO inhibitors.
- Medication overuse headache: Using acute headache treatments on too many days per month can cause headaches to become more frequent and harder to treat.
- Seizures: Seizures have been reported; use with caution if you have epilepsy or a condition that lowers your seizure threshold.
Sumatriptan interactions
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Sumatriptan has several important drug interactions that can be dangerous:
- Ergot-containing drugs (e.g., dihydroergotamine, methysergide) — cannot be used within 24 hours of sumatriptan; both cause blood vessel constriction and the effects are additive
- Other triptans or 5-HT1 agonists — cannot be combined within 24 hours; same reason as ergots
- MAO-A inhibitors — cannot be used together or within 2 weeks; they dramatically increase sumatriptan levels in the blood (up to 7-fold), raising the risk of serious side effects
- SSRIs, SNRIs, tricyclic antidepressants, and MAO inhibitors — using these together with sumatriptan raises the risk of serotonin syndrome
Interactions listed in the FDA-approved label
From the Sumatriptan prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Ergot-containing drugs (ergotamine, dihydroergotamine, methysergide): Ergot-containing drugs have been reported to cause prolonged vasospastic reactions, and these effects may be additive. Use within 24 hours of each other is contraindicated.
- Monoamine oxidase-A (MAO-A) inhibitors: MAO-A inhibitors increase systemic exposure by up to 7-fold. Use in patients receiving MAO-A inhibitors is contraindicated.
- Other 5-HT1 agonists (e.g., triptans): Their vasospastic effects may be additive. Coadministration within 24 hours of each other is contraindicated.
- SSRIs, SNRIs, TCAs and MAO inhibitors: Cases of serotonin syndrome have been reported during coadministration of triptans with these drugs.
Read the label’s full interactions text
7 DRUG INTERACTIONS 7.1 Ergot-Containing Drugs Ergot-containing drugs have been reported to cause prolonged vasospastic reactions. Because these effects may be additive, use of ergotamine-containing or ergot-type medications (like dihydroergotamine or methysergide) and sumatriptan succinate tablets within 24 hours of each other is contraindicated. 7.2 Monoamine Oxidase-A Inhibitors MAO-A inhibitors increase systemic exposure by 7-fold. Therefore, the use of sumatriptan succinate tablets in patients receiving MAO-A inhibitors is contraindicated [see Clinical Pharmacology ( 12.3 )] . 7.3 Other 5-HT1 Agonists Because their vasospastic effects may be additive, coadministration of sumatriptan succinate tablets and other 5-HT 1 agonists (e.g., triptans) within 24 hours of each other is contraindicated. 7.4 Selective Serotonin Reuptake Inhibitors/Serotonin Norepinephrine Reuptake Inhibitors and Serotonin Syndrome Cases of serotonin syndrome have been reported during coadministration of triptans and SSRIs, SNRIs, TCAs, and MAO inhibitors [see Warnings and Precautions ( 5.7 )] .
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Sumatriptan
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- Tell your prescriber if you have any history of heart disease, angina, heart attack, or arrhythmias such as Wolff-Parkinson-White syndrome
- Tell your prescriber if you have had a stroke, TIA (mini-stroke), or certain types of migraine (hemiplegic or basilar) — sumatriptan is contraindicated in these cases
- Tell your prescriber if you have peripheral vascular disease, ischemic bowel disease, or uncontrolled high blood pressure
- Tell your prescriber if you have liver disease — tablets are contraindicated in severe liver impairment; dose limits apply for mild to moderate impairment
- Tell your prescriber about all other medications, especially antidepressants and any MAO inhibitors
- Pregnancy: Animal studies showed possible fetal harm; discuss the risks and benefits with your doctor before using
- Breastfeeding: Sumatriptan passes into breast milk; consider avoiding nursing for 12 hours after a dose to reduce infant exposure
- Children and adolescents under 18: Effectiveness has not been established; not recommended for this age group
- Older adults: Use cautiously; a cardiovascular evaluation is recommended if heart risk factors are present
- Latex-sensitive patients: the needle shield on some prefilled syringes (Imitrex and Sumatriptan Succinate injection) contains natural rubber latex — alert your provider
Sumatriptan overdose
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If too much sumatriptan is taken, watch for signs such as seizures, tremor, weakness or paralysis, breathing problems, and bluish skin color. The drug has a short half-life of about 2.5 hours, but monitoring should continue for at least 10 hours after an overdose or while any symptoms persist. If you suspect an overdose, contact poison control or seek emergency medical care immediately.
What Sumatriptan does in the body
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Sumatriptan causes constriction of cranial blood vessels by activating 5-HT1B/1D receptors. Studies in healthy volunteers did not find a clinically significant increase in resistance in small peripheral (outer body) arteries at therapeutic doses. However, significant rises in blood pressure — including hypertensive crisis — have been reported in some patients, with and without a history of high blood pressure. Changes in blood pressure during clinical trials were generally not accompanied by significant changes in heart rate.
How your body processes Sumatriptan
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When taken by mouth, sumatriptan has an oral bioavailability (the fraction that actually reaches the bloodstream) of only about 15%, mainly because the liver breaks much of it down before it enters circulation. Blood levels peak later during a migraine attack than during a headache-free period. Sumatriptan is broken down primarily by an enzyme called MAO-A, mostly in the liver, and the resulting breakdown products are inactive; only about 3% of a dose leaves the body unchanged. The elimination half-life — the time it takes the body to clear half the drug — is approximately 2.5 hours, with most of the drug leaving through the urine and some through the stool. In people with liver disease, blood levels can be significantly higher than normal, which is why dose adjustments are needed and tablets are contraindicated in severe liver impairment.
How to store Sumatriptan
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Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) (See USP controlled Room Temperature.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Sumatriptan
50 supplements and herbal products have documented interactions with Sumatriptan in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 8
- Moderate · 31
- Minor · 11
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Sumatriptan: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Sumatriptan — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly does sumatriptan do — does it prevent migraines or stop them?
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When should I take it during a migraine attack?
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What side effects should I just expect, and which ones mean I should call for help?
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Can I take sumatriptan with my antidepressant?
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Is it safe to use sumatriptan if I'm pregnant or breastfeeding?
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I've been getting more headaches lately — could sumatriptan itself be causing them?
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Is Sumatriptan available over the counter?
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When was Sumatriptan first available?
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Who makes Sumatriptan?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Sumatriptan on HelloPharmacist
Sumatriptan forms and strengths (how it comes)
Sumatriptan is available in 3 forms. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Tablet
How this form is used
- Imitrex tablets: acute treatment of migraine with or without aura in adults
- Sumatriptan tablets: acute treatment of migraine with or without aura in adults
- Tablets are not indicated for cluster headache or for migraine prevention
- Taken by mouth, with or without food
- If the migraine has not resolved or returns after 2 hours, a second dose may be taken — but only if the first dose provided some relief
- Do not exceed the maximum daily amount in a 24-hour period
- In patients with mild to moderate liver impairment, the maximum single dose is limited — follow your prescriber's guidance
Injection
How this form is used
- Imitrex injection: acute treatment of migraine with or without aura in adults, and acute treatment of cluster headache in adults
- Sumatriptan injection: acute treatment of migraine with or without aura in adults, and acute treatment of cluster headache in adults
- Sumatriptan Succinate injection: acute treatment of migraine with or without aura in adults, and acute treatment of cluster headache in adults
- Zembrace SymTouch: acute treatment of migraine with or without aura in adults only — not indicated for cluster headache
- For subcutaneous (under the skin) use only — do not inject by any other route
- Zembrace SymTouch is a prefilled single-dose auto-injector; the needle penetrates approximately ¼ inch
- A second injection should only be considered if the first dose provided some relief; separate doses by at least 1 hour
- The needle shield of Imitrex and Sumatriptan Succinate prefilled syringes contains natural rubber latex — tell your doctor if you have a latex allergy
Nasal spray
How this form is used
- Imitrex nasal spray: acute treatment of migraine with or without aura in adults
- Sumatriptan nasal spray: acute treatment of migraine with or without aura in adults
- Tosymra: acute treatment of migraine with or without aura in adults
- Nasal spray forms are not indicated for cluster headache or migraine prevention
- Tosymra is given as a single spray into one nostril
- Tosymra: the maximum cumulative dose in 24 hours is 30 mg; separate doses by at least 1 hour
- Nasal and throat irritation, burning, or numbness may occur after use and typically resolves within 2 hours
- Do not use more frequently than directed; follow your prescriber's instructions
Show 3 more strengths Show fewer strengths
Sumatriptan on the U.S. market: products, makers and brands
How Sumatriptan appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
42 companies list 122 Sumatriptan product records with the FDA, mostly as tablet, injection, nasal spray; the earliest marketing or approval year on record is 1992. Brand names on the directory include Imitrex Tablets, Zembrace, Onzetra and 3 more; the rest are generics.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (21) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Sumatriptan is used (Medicaid data)
A general measure of how commonly Sumatriptan is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Sumatriptan is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Sumatriptan prescribed? Of the 1,601 medications we measure, Sumatriptan ranks #130 by Medicaid prescriptions — more than 92% of them.
Utilization by Sumatriptan product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
sumatriptan 50 MG Oral Tablet Most dispensed
Summed across the 13 of 76 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 313161
sumatriptan 100 MG Oral Tablet
Summed across the 13 of 70 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 313160
sumatriptan 25 MG Oral Tablet
Summed across the 11 of 71 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 315223
sumatriptan 20 MG/ACTUAT Nasal Spray
Summed across the 5 of 9 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 314227
0.5 ML sumatriptan 12 MG/ML Auto-Injector
Summed across the 4 of 23 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1657151
sumatriptan 5 MG/ACTUAT Nasal Spray
Summed across the 3 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 313159
0.5 ML sumatriptan 12 MG/ML Injection
Summed across the 5 of 30 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 313165
0.5 ML sumatriptan 12 MG/ML Cartridge
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1657160
sumatriptan 10 MG/ACTUAT Nasal Spray
Summed across the 2 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 401978
0.5 ML sumatriptan 6 MG/ML Auto-Injector
Summed across the 2 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1738576
0.5 ML sumatriptan 8 MG/ML Cartridge
Summed across the 1 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1657173
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Sumatriptan, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 61 of 311 listed Sumatriptan NDCs with Medicaid activity.
Compare Sumatriptan products
A representative set of FDA-listed product records for Sumatriptan — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| 6 mg/0.5 mL | Subcutaneous | A-S Medication Solutions × 2 listings | ANDA | View NDC → |
| 4 mg/0.5 mL | Subcutaneous | Alembic Pharmaceuticals Inc. | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Alembic Pharmaceuticals Inc. | ANDA | View NDC → |
| 4 mg/0.5 mL | Subcutaneous | Alembic Pharmaceuticals Limited | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Alembic Pharmaceuticals Limited | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Armas Pharmaceuticals Inc. | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Baxter Healthcare Corporation | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Caplin Steriles Limited | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Dr. Reddys Laboratories Inc., | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Eugia US LLC | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Fresenius Kabi USA, LLC | ANDA | View NDC → |
| 4 mg/0.5 mL | Subcutaneous | GlaxoSmithKline LLC | NDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | GlaxoSmithKline LLC × 2 listings | NDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Golden State Medical Supply, Inc. | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | NorthStar Rx LLC | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Onesource Specialty Pharma Limited × 4 listings | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Proficient Rx LP | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Sportpharm LLC × 2 listings | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Strides Pharma Science Limited | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 4 mg/0.5 mL | Subcutaneous | Teva Pharmaceuticals USA Inc | ANDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Teva Pharmaceuticals USA Inc | ANDA | View NDC → |
| 3 mg/0.5 mL | Subcutaneous | Tonix Medicines, Inc. | NDA | View NDC → |
| 6 mg/0.5 mL | Subcutaneous | Xellia Pharmaceuticals USA LLC | ANDA | View NDC → |
| 💊Nasal spray | ||||
| 5 mg | Nasal | Bryant Ranch Prepack | ANDA | View NDC → |
| 20 mg | Nasal | Bryant Ranch Prepack | ANDA | View NDC → |
| 20 mg | Nasal | Cipla USA Inc. | ANDA | View NDC → |
| 20 mg | Nasal | Florida Pharmaceutical Products, LLC. | ANDA | View NDC → |
| 5 mg/0.1 mL | Nasal | Lannett Company, Inc. | ANDA | View NDC → |
| 20 mg/0.1 mL | Nasal | Lannett Company, Inc. | ANDA | View NDC → |
| 5 mg | Nasal | Padagis Israel Pharmaceuticals Ltd | ANDA | View NDC → |
| 20 mg | Nasal | Padagis Israel Pharmaceuticals Ltd | ANDA | View NDC → |
| SUMATRIPTAN 5 mg/100uL | Nasal | Prasco Laboratories | NDA AUTHORIZED GENERIC | View NDC → |
| SUMATRIPTAN 20 mg/100uL | Nasal | Prasco Laboratories | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg/0.1 mL | Nasal | Tonix Medicines, Inc. | NDA | View NDC → |
| 10 mg/0.1 mL | Nasal | Upsher-Smith Laboratories, LLC | NDA | View NDC → |
| 💊Tablet | ||||
| 25 mg | Oral | A-S Medication Solutions × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | A-S Medication Solutions | ANDA | View NDC → |
| 100 mg | Oral | A-S Medication Solutions | ANDA | View NDC → |
| 50 mg | Oral | Advanced Rx of Tennessee, LLC | ANDA | View NDC → |
| 100 mg | Oral | Advanced Rx of Tennessee, LLC | ANDA | View NDC → |
| 50 mg | Oral | Advanced Rx Pharmacy of Tennessee, LLC | ANDA | View NDC → |
| 100 mg | Oral | Advanced Rx Pharmacy of Tennessee, LLC | ANDA | View NDC → |
| 25 mg | Oral | Asclemed USA, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Asclemed USA, Inc. × 2 listings | ANDA | View NDC → |
| 100 mg | Oral | Asclemed USA, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 50 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 100 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 25 mg | Oral | Bionpharma Inc. | ANDA | View NDC → |
| 50 mg | Oral | Bionpharma Inc. | ANDA | View NDC → |
| 100 mg | Oral | Bionpharma Inc. | ANDA | View NDC → |
| 25 mg | Oral | Direct_Rx × 2 listings | ANDA | View NDC → |
| 50 mg | Oral | Direct_Rx | ANDA | View NDC → |
| 100 mg | Oral | Direct_Rx | ANDA | View NDC → |
| 25 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 50 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 100 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 25 mg | Oral | GlaxoSmithKline LLC | NDA | View NDC → |
| 50 mg | Oral | GlaxoSmithKline LLC | NDA | View NDC → |
| 100 mg | Oral | GlaxoSmithKline LLC | NDA | View NDC → |
| 25 mg | Oral | NorthStar Rx LLC | ANDA | View NDC → |
| 50 mg | Oral | NorthStar Rx LLC | ANDA | View NDC → |
| 100 mg | Oral | NorthStar Rx LLC | ANDA | View NDC → |
| 50 mg | Oral | NuCare Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mg | Oral | NuCare Pharmaceuticals,Inc. × 3 listings | ANDA | View NDC → |
| 100 mg | Oral | NuCare Pharmaceuticals, Inc. | ANDA | View NDC → |
| 100 mg | Oral | NuCare Pharmaceuticals,Inc. × 2 listings | ANDA | View NDC → |
| 50 mg | Oral | Preferred Pharmaceuticals, Inc. | ANDA | View NDC → |
| 100 mg | Oral | Preferred Pharmaceuticals, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Preferred Pharmaceuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | Proficient Rx LP × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | Proficient Rx LP × 2 listings | ANDA | View NDC → |
| 100 mg | Oral | Proficient Rx LP × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | Quality Care Products, LLC | ANDA | View NDC → |
| 100 mg | Oral | Quality Care Products, LLC | ANDA | View NDC → |
| 100 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 25 mg | Oral | Sportpharm LLC | ANDA | View NDC → |
| 50 mg | Oral | Sportpharm LLC | ANDA | View NDC → |
| 100 mg | Oral | Sportpharm LLC | ANDA | View NDC → |
| 25 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 100 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
Showing 104 of 122 products — FDA National Drug Code Directory. See every product, package size and price: browse all 122 Sumatriptan NDCs →
Sumatriptan side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Sumatriptan — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Sumatriptan in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Sumatriptan FDA approval history
How Sumatriptan went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Sumatriptan recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list one Sumatriptan recall since July 2021. It is no longer listed as ongoing. A recall names specific lots from one company, so check the lot number on your own bottle rather than assuming every product is affected; your pharmacist can check whether your supply came from an affected lot.
- Sumatriptan Succinate Tablets, 100 mg, 9 (1 x 9) Unit-of- use tablets box, Rx only, MFG: Sun Pharmaceuticals, NDC 62756-522-69 Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that i… FDA record D-1111-2022 →
Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 37418 8 dose forms · 15 strengths
-
Dose form (SCDF) Auto-Injector RxCUI 1657150In current FDA listingsClinical drug / strength (SCD) 0.5 ML sumatriptan 12 MG/MLRxCUI 16571510.5 ML sumatriptan 6 MG/MLRxCUI 17385760.5 ML sumatriptan 8 MG/MLRxCUI 1793916 -
Dose form (SCDF) Cartridge RxCUI 1657159No current FDA listingClinical drug / strength (SCD) 0.5 ML sumatriptan 12 MG/MLRxCUI 16571600.5 ML sumatriptan 8 MG/MLRxCUI 1657173 -
Dose form (SCDF) Injection RxCUI 1656981In current FDA listingsClinical drug / strength (SCD) 0.5 ML sumatriptan 12 MG/MLRxCUI 3131650.5 ML sumatriptan 8 MG/MLRxCUI 1657010 -
Dose form (SCDF) Nasal Powder RxCUI 1739331No current FDA listingClinical drug / strength (SCD) 11 MGRxCUI 1739332 -
Dose form (SCDF) Nasal Spray RxCUI 379118In current FDA listingsClinical drug / strength (SCD) 5 MG/ACTUATRxCUI 31315910 MG/ACTUATRxCUI 40197820 MG/ACTUATRxCUI 314227 -
Dose form (SCDF) Oral Tablet RxCUI 374012In current FDA listings -
Dose form (SCDF) Prefilled Syringe RxCUI 727338No current FDA listingClinical drug / strength (SCD) 0.5 ML sumatriptan 12 MG/MLRxCUI 727339 -
Dose form (SCDF) Transdermal System RxCUI 1806101No current FDA listing
Look up RxCUI 37418 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Sumatriptan supply and shortage status
Whether Sumatriptan is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Sumatriptan costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet · Oral | 100 mg | $0.439 per tablet | NDC details & price history |
| Tablet · Oral | 50 mg | $0.302 per tablet | NDC details & price history |
| Tablet · Oral | 25 mg | $0.239 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 50 mg | $73.07 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 100 mg | $72.40 per tablet | NDC details & price history |
| Injection · Subcutaneous | 6 mg/0.5 mL | $14.93 per mL | NDC details & price history |
| Injection · Subcutaneous | 4 mg/0.5 mL | $463.07 per mL | NDC details & price history |
| Spray · Nasal | 20 mg | $16.51 each | NDC details & price history |
| Spray · Nasal | 5 mg | $17.04 each | NDC details & price history |
| Spray · Nasal | SUMATRIPTAN 5 mg/100uL | $17.04 each | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Sumatriptan brand names
Sumatriptan is sold under 6 brand names in the FDA directory — Imitrex Tablets, Zembrace, Onzetra, Imitrex and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Sumatriptan: manufacturers and labelers
42 companies list Sumatriptan products with the FDA. By number of product records, the largest are Proficient Rx LP, NuCare Pharmaceuticals,Inc., A-S Medication Solutions. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
…and 18 more on the FDA NDC directory.
Sumatriptan drug class (RxNorm)
Sumatriptan belongs to the Serotonin-1b and Serotonin-1d Receptor Agonist class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Sumatriptan page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. GlaxoSmithKline LLC is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →