Zolmitriptan
Zolmitriptan is a triptan medication used to treat acute migraine attacks — with or without aura — in adults, and in patients 12 and older when used as a nasal spray.
🧬 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 22 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 →
📖 Zolmitriptan: Patient Information Guide
A plain-language walkthrough of Zolmitriptan — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Zolmitriptan is used to treat acute migraine attacks across several product forms. It is not used to prevent migraines — only to stop one that has already started.
- Zomig tablets and Zolmitriptan tablets: acute migraine with or without aura in adults
- Zolmitriptan orally disintegrating tablets and Zolmitriptan OD: acute migraine with or without aura in adults
- Zomig Nasal Spray and Zolmitriptan Nasal Spray: acute migraine with or without aura in adults and adolescents 12 years and older
- All forms: only use when a clear migraine diagnosis has already been made by a healthcare provider
- No form is approved for cluster headaches or migraine prevention
- Nasal spray forms are not recommended in patients with moderate to severe liver impairment
⚙️How it works▾
Zolmitriptan is a triptan — it works by attaching to serotonin receptors (specifically 5-HT1B and 5-HT1D receptors) found on blood vessels in the brain and on the trigeminal nerves that drive migraine pain. By activating these receptors, it causes widened cranial blood vessels to constrict (narrow back down) and blocks the release of pain-promoting chemicals from nerve endings. Both actions help relieve the throbbing pain and associated symptoms of a migraine attack. The body also converts zolmitriptan into an active breakdown product that targets the same receptors and may contribute meaningfully to the overall effect.
💊How it's taken▾
Zolmitriptan is taken at the first sign of a migraine — the sooner, the better. Tablets and orally disintegrating tablets are taken by mouth; nasal spray is used in the nose. If the migraine has not resolved or comes back after 2 hours, a second dose may be taken — but always wait at least 2 hours between doses and stay within your daily limit. Food does not significantly affect how zolmitriptan is absorbed. Use only as directed by your prescriber; the safety of treating more than about four migraines per month has not been established.
- Tablets and orally disintegrating tablets: taken orally; may be taken with or without food
- Nasal spray: administered into the nose; individual response may vary and dose can be adjusted by your prescriber
- Liver impairment: lower doses are recommended for moderate to severe hepatic impairment with tablets; nasal spray is not recommended in this group
🤒Side effects — in detail▾
The most common side effects reported in clinical trials include:
- Tingling or numbness (paresthesia)
- Neck, throat, or jaw pain, tightness, or pressure
- Dizziness
- Drowsiness (somnolence)
- Nausea
- Warm or cold sensations
- Dry mouth
- Feelings of heaviness or weakness (asthenia)
- Sweating
Chest tightness, pressure, or pain can also occur and is usually not cardiac in origin — but if you have heart disease risk factors, tell your doctor right away. Rare but serious reactions include heart rhythm problems, stroke, severe allergic reactions (including swelling of the face or throat), and serotonin syndrome — seek emergency care immediately if any of these occur.
⚠️Warnings & precautions▾
- Cardiovascular risk: Rare but serious cardiac events — including heart attack and dangerous heart rhythms — have occurred shortly after use, even in people without known heart disease. A cardiac evaluation is recommended before use in anyone with multiple heart disease risk factors.
- Stroke and cerebrovascular events: Cerebral hemorrhage and stroke have been reported. Zolmitriptan is contraindicated in anyone with a history of stroke or TIA.
- Serotonin syndrome: A life-threatening reaction can occur when zolmitriptan is combined with certain antidepressants (SSRIs, SNRIs, MAO inhibitors). Symptoms include agitation, high fever, rapid heartbeat, and muscle twitching — stop taking it and get help immediately.
- Medication overuse headache: Using any acute migraine drug too frequently (10 or more days per month) can cause headaches to worsen or become more frequent. If this happens, withdrawal and detoxification under medical supervision may be needed.
- Blood pressure increases: Significant blood pressure elevations have been reported, especially in patients with liver impairment. Blood pressure should be monitored during treatment.
- Vasospasm reactions: Beyond the heart, blood vessel spasm can affect the gut (causing abdominal pain and bloody diarrhea), the limbs, and other areas. Stop use and contact your doctor if these symptoms occur.
🔀What it interacts with▾
Zolmitriptan interacts with several drug types — some of these combinations are contraindicated (meaning they must be avoided):
- Ergot-containing drugs (e.g., dihydroergotamine, methysergide) — do not use within 24 hours; both narrow blood vessels and the combined effect can be dangerous
- Other triptans or 5-HT1 agonists — do not use within 24 hours; additive risk of blood vessel spasm
- MAO-A inhibitors (certain antidepressants) — do not use together or within 2 weeks of stopping; zolmitriptan levels increase significantly, raising toxicity risk
- SSRIs and SNRIs (many common antidepressants) — combination raises risk of serotonin syndrome, a potentially life-threatening condition
- Cimetidine (a heartburn/ulcer drug) — approximately doubles zolmitriptan blood levels; dose adjustment is required if used together
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Tell your prescriber if you have any heart disease, coronary artery disease, history of heart attack, chest pain (angina), or Wolff-Parkinson-White syndrome
- Tell your prescriber if you have had a stroke, TIA (mini-stroke), or have hemiplegic or basilar migraine — zolmitriptan is contraindicated in these cases
- Tell your prescriber if you have uncontrolled high blood pressure — this is a contraindication
- Tell your prescriber if you have peripheral vascular disease or ischemic bowel disease
- Tell your prescriber if you have moderate or severe liver disease — nasal spray forms are not recommended, and oral doses may need to be lowered
- Pregnancy: Animal studies showed potential for fetal harm; there are no adequate human data. Discuss the risks and benefits with your prescriber if you are or plan to become pregnant
- Breastfeeding: It is not known if zolmitriptan passes into human breast milk; discuss with your prescriber before breastfeeding
- Children: Not approved for patients under 12; nasal spray has established safety and efficacy in ages 12 to 17
- Older adults: Use cautiously; a cardiovascular evaluation is recommended if heart disease risk factors are present
- Do not use zolmitriptan if you have had a serious allergic reaction (anaphylaxis, angioedema) to it before
🚑If you take too much▾
There is limited experience with zolmitriptan overdose. In clinical studies, subjects who took a single very large oral dose commonly experienced heavy sedation. There is no specific antidote. If an overdose is suspected, seek emergency care — supportive treatment including monitoring of breathing and heart function is recommended. Because zolmitriptan's half-life is about 3 hours, patients should be monitored for at least 15 hours or until symptoms fully resolve.
📡Pharmacodynamics — effects in the body▾
Zolmitriptan activates 5-HT1B/1D serotonin receptors on intracranial blood vessels and trigeminal nerve endings. This causes cranial blood vessels to narrow (constrict) and blocks the release of pain-promoting neuropeptides, which are chemicals involved in migraine inflammation. The result is relief of migraine headache pain and associated symptoms. Zolmitriptan can also raise blood pressure, and this effect may be more pronounced in patients with liver impairment.
🔬Pharmacokinetics — how your body processes it▾
When given as a nasal spray, zolmitriptan is rapidly absorbed through the nasal passages and can be detected in the blood within 5 minutes; peak blood levels are typically reached around 3 hours. The nasal spray has bioavailability comparable to the oral tablet. Food does not meaningfully affect absorption of the oral form. Zolmitriptan is converted in the body to an active metabolite that is 2 to 6 times more potent at the target receptors. Both zolmitriptan and its active metabolite have an elimination half-life of about 3 hours, and the drug is cleared mainly through the urine and feces. Blood levels can be significantly higher in patients with severe liver disease, and women tend to have somewhat higher plasma concentrations than men.
📦How to store it▾
Store at 20°C to 25°C (68°F to 77°F) . Protect from light and moisture. Dispense in a tight, light-resistant closed container.
📄 Written from Zolmitriptan’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
Supplements & herbs that interact with Zolmitriptan
50 supplements and herbal products have documented interactions with Zolmitriptan 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.
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Zolmitriptan — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly does zolmitriptan do — will it stop my migraine or just take the edge off? ▾
Can I take it again if my headache comes back a few hours later? ▾
What side effects should I actually expect, and which ones should make me call someone? ▾
Are there medications I absolutely cannot take with this? ▾
I'm pregnant — is it safe to use this for migraines? ▾
Can my teenager use zolmitriptan nasal spray? ▾
Is Zolmitriptan available over the counter? ▾
When was Zolmitriptan first available? ▾
Who makes Zolmitriptan? ▾
💬 Answers drafted from Zolmitriptan’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Zolmitriptan comes
Zolmitriptan 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
- Zomig tablets are approved for acute treatment of migraine with or without aura in adults
- Zolmitriptan tablets are approved for acute treatment of migraine with or without aura in adults
- Not approved for migraine prevention or cluster headaches
- Zomig tablets and Zolmitriptan tablets are taken by mouth at the onset of a migraine; food does not significantly affect absorption
- The 2.5 mg tablet is scored and can be broken in half to achieve a lower starting dose if directed by a prescriber
- A second dose may be taken at least 2 hours after the first if the migraine has not resolved or returns
- Patients with moderate or severe liver impairment should use a lower starting dose as directed by their prescriber
Orally disintegrating tablet
How this form is used
- Zolmitriptan orally disintegrating tablets are approved for acute treatment of migraine with or without aura in adults
- Zolmitriptan OD orally disintegrating tablets are approved for acute treatment of migraine with or without aura in adults
- Not approved for migraine prevention or cluster headaches
- Orally disintegrating tablets are taken by mouth and dissolve on the tongue — do not break the tablet
- A second dose may be taken at least 2 hours after the first if the migraine has not resolved or returns
- Do not exceed the maximum daily limit in any 24-hour period — follow your prescriber's guidance
- Patients with moderate or severe liver impairment should use a lower starting dose as directed by their prescriber
Nasal spray
How this form is used
- Zomig Nasal Spray is approved for acute treatment of migraine with or without aura in adults and adolescents 12 years of age and older
- Zolmitriptan Nasal Spray is approved for acute treatment of migraine with or without aura in adults and adolescents 12 years of age and older
- Not approved for migraine prevention or for cluster headaches
- Not recommended in patients with moderate to severe liver impairment
- Zomig Nasal Spray and Zolmitriptan Nasal Spray are administered into the nose at the onset of a migraine
- A second dose may be given at least 2 hours after the first if the migraine has not resolved or returns
- Do not exceed the maximum daily amount in any 24-hour period — follow your prescriber's instructions
- Safety for treating more than four migraines per 30-day period has not been established
📊 Zolmitriptan across the U.S. market
How Zolmitriptan 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.
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 (10) — 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 Zolmitriptan is used
A general measure of how commonly Zolmitriptan 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 Zolmitriptan 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 Zolmitriptan prescribed? Of the 1,596 medications we measure, Zolmitriptan ranks #756 by Medicaid prescriptions — more than 53% of them.
Utilization by Zolmitriptan 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.
zolmitriptan 5 MG Oral Tablet Most dispensed
Summed across the 6 of 29 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 200194
zolmitriptan 5 MG/ACTUAT Nasal Spray
Summed across the 3 of 12 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 402000
zolmitriptan 5 MG Disintegrating Oral Tablet
Summed across the 3 of 25 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 351134
zolmitriptan 2.5 MG Oral Tablet
Summed across the 4 of 29 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 200193
zolmitriptan 2.5 MG Disintegrating Oral Tablet
Summed across the 3 of 25 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 284201
zolmitriptan 2.5 MG/ACTUAT Nasal Spray
Summed across the 2 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1483677
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 Zolmitriptan, 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 21 of 123 listed Zolmitriptan NDCs with Medicaid activity.
🔍 Compare Zolmitriptan products
A representative set of FDA-listed product records for Zolmitriptan — 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 |
|---|---|---|---|---|
| 💊Nasal spray | ||||
| 2.5 mg | Nasal | Amneal Pharmaceuticals | NDA | View NDC → |
| 2.5 mg | Nasal | Amneal Pharmaceuticals | NDA AUTHORIZED GENERIC | View NDC → |
| 5 mg | Nasal | Amneal Pharmaceuticals | NDA | View NDC → |
| 5 mg | Nasal | Amneal Pharmaceuticals | NDA AUTHORIZED GENERIC | View NDC → |
| 2.5 mg | Nasal | Amneal Pharmaceuticals LLC | NDA | View NDC → |
| 5 mg | Nasal | Amneal Pharmaceuticals LLC | NDA | View NDC → |
| 2.5 mg | Nasal | Amneal Pharmaceuticals NY LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 5 mg | Nasal | Amneal Pharmaceuticals NY LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 5 mg | Nasal | Bryant Ranch Prepack × 4 listings | ANDA | View NDC → |
| 5 mg | Nasal | Padagis Israel Pharmaceuticals Ltd × 2 listings | ANDA | View NDC → |
| 💊Orally disintegrating tablet | ||||
| 2.5 mg | Oral | Alembic Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Alembic Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Alembic Pharmaceuticals Limited × 3 listings | ANDA | View NDC → |
| 5 mg | Oral | Alembic Pharmaceuticals Limited × 3 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Amneal Pharmaceuticals | NDA | View NDC → |
| 5 mg | Oral | Amneal Pharmaceuticals | NDA | View NDC → |
| 2.5 mg | Oral | AvKARE | ANDA | View NDC → |
| 5 mg | Oral | AvKARE | ANDA | View NDC → |
| 2.5 mg | Oral | Glenmark Pharmaceuticals Inc., USA × 3 listings | ANDA | View NDC → |
| 5 mg | Oral | Glenmark Pharmaceuticals Inc., USA × 3 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | View NDC → |
| 5 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Jubilant Cadista Pharmacuticals Inc. | ANDA | View NDC → |
| 5 mg | Oral | Jubilant Cadista Pharmacuticals Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Rising Pharmaceuticals, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Rising Pharmaceuticals, Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Zydus Lifesciences Limited × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Zydus Lifesciences Limited × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Zydus Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Zydus Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 💊Tablet | ||||
| 2.5 mg | Oral | Ajanta Pharma USA Inc. × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Ajanta Pharma USA Inc. × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Alembic Pharmaceuticals Inc. | ANDA | View NDC → |
| 5 mg | Oral | Alembic Pharmaceuticals Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Alembic Pharmaceuticals Limited × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Alembic Pharmaceuticals Limited × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Amneal Pharmaceuticals | NDA | View NDC → |
| 5 mg | Oral | Amneal Pharmaceuticals | NDA | View NDC → |
| 2.5 mg | Oral | Amneal Pharmaceuticals LLC × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Amneal Pharmaceuticals LLC × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Asclemed USA, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Asclemed USA, Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Aurobindo Pharma Limited × 3 listings | ANDA | View NDC → |
| 5 mg | Oral | Aurobindo Pharma Limited × 3 listings | ANDA | View NDC → |
| 2.5 mg | Oral | BluePoint Laboratories × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | BluePoint Laboratories × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Celltrion Usa, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Celltrion Usa, Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Cipla USA Inc. | ANDA | View NDC → |
| 5 mg | Oral | Cipla USA Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Curae Pharma360 Inc | ANDA | Find on DailyMed ↗ |
| 2.5 mg | Oral | Direct_Rx × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Direct_Rx × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Glenmark Pharmaceuticals Inc.,USA × 3 listings | ANDA | View NDC → |
| 5 mg | Oral | Glenmark Pharmaceuticals Inc.,USA × 3 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Ingenus Pharmaceuticals, LLC | ANDA | Find on DailyMed ↗ |
| 5 mg | Oral | Ingenus Pharmaceuticals, LLC | ANDA | Find on DailyMed ↗ |
| 2.5 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | Find on DailyMed ↗ |
| 5 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | Find on DailyMed ↗ |
| 2.5 mg | Oral | Medstone Pharma LLC × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Medstone Pharma LLC × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | PLD Acquisitions LLC DBA Avma Pharma Solutions | ANDA | View NDC → |
| 2.5 mg | — | PLD Acquisitions LLC DBA Avma Pharma Solutions | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 5 mg | Oral | PLD Acquisitions LLC DBA Avma Pharma Solutions | ANDA | View NDC → |
| 5 mg | — | PLD Acquisitions LLC DBA Avma Pharma Solutions | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 2.5 mg | Oral | PLD Acquisitions LLC DBA Av�ma Pharma Solutions | ANDA | View NDC → |
| 5 mg | Oral | PLD Acquisitions LLC DBA Av�ma Pharma Solutions | ANDA | View NDC → |
| 2.5 mg | Oral | Quality Care Products, LLC | ANDA | View NDC → |
| 5 mg | Oral | Quality Care Products, LLC | ANDA | View NDC → |
| 2.5 mg | Oral | Rising Pharmaceuticals, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Rising Pharmaceuticals, Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Rising Pharma Holdings, Inc. × 2 listings | ANDA | View NDC → |
| 5 mg | Oral | Rising Pharma Holdings, Inc. × 2 listings | ANDA | View NDC → |
| 2.5 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 5 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 2.5 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 5 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 💊Bulk drug substance | ||||
| 1 kg/kg | — | Alivus Life Sciences Limited | BULK INGREDIENT | View NDC → |
| 50 kg/50 kg | — | Aurobindo Pharma Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Dr.Reddy's Laboratories Limited | BULK INGREDIENT | View NDC → |
| 5 kg/5 kg | — | Emcure Pharmaceuticals Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Hetero Drugs Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Inke Sa | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Jubilant Biosys limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Matrix Pharmacorp Private Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Natco Pharma Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | SMS Pharmaceuticals Limited | BULK INGREDIENT | View NDC → |
Showing 127 of 127 products — FDA National Drug Code Directory. See every product, package size and price: browse all 127 Zolmitriptan NDCs →
📈 What people report — real-world data (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 Zolmitriptan — 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 Zolmitriptan 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.
🏛️ The road to your pharmacy
How Zolmitriptan went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 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.
Source: openFDA drug enforcement (recall) reports.
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 135775 3 dose forms · 6 strengths
-
Dose form (SCDF) Disintegrating Oral Tablet RxCUI 374653In current FDA listings -
Dose form (SCDF) Nasal Spray RxCUI 402420In current FDA listings -
Dose form (SCDF) Oral Tablet RxCUI 374363In current FDA listings
Look up RxCUI 135775 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.
📦 Supply & shortage status
Whether Zolmitriptan 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.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
…and 14 more on the FDA NDC directory.
RxNorm drug class
Zolmitriptan 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.
🔬 Where this comes from
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 we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 22 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. PLD Acquisitions LLC DBA Av�ma Pharma Solutions is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.