Meclizine
Meclizine is an antihistamine used to prevent and treat nausea, vomiting, and dizziness from motion sickness, and to treat vertigo caused by inner ear disorders.
🧬 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 163 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 →
📖 Meclizine: Patient Information Guide
A plain-language walkthrough of Meclizine — 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▾
Meclizine is an antihistamine used for two main purposes across its many available products.
- Motion sickness: Prevention and treatment of nausea, vomiting, and dizziness caused by motion sickness — supported across all meclizine products, including Bonine, Bonine Max, Dramamine, Dramamine Less Drowsy, Dramamine-N, Naus-ease, CVS Motion Sickness Fast Melting, Wal-Dram 2 Quick-Dissolving, Meclizine HCL, and others.
- Vertigo: Treatment of vertigo (a spinning or whirling sensation) associated with diseases affecting the vestibular system — the inner ear balance system — in adults. This is an indication for prescription meclizine hydrochloride tablets, as well as Naus-ease tablets and film strips.
⚙️How it works▾
Meclizine is thought to work primarily by blocking histamine H1 receptors — sites in the body where histamine normally binds and triggers responses like nausea, vomiting, and dizziness. By blocking these receptors, meclizine helps calm those symptoms. The exact full mechanism isn't completely understood, but this antihistamine action is considered the core of how it helps with motion sickness and vestibular-related dizziness. Meclizine also has anticholinergic properties, meaning it can block certain nerve signals, which may contribute to both its effects and some of its side effects.
💊How it's taken▾
Meclizine is taken by mouth. For motion sickness, take it about one hour before travel and then once every 24 hours as needed during the trip. For vertigo, prescription meclizine hydrochloride tablets are taken in divided doses daily, as directed by your doctor — the amount depends on how well the condition is responding.
- Standard tablets: Swallow whole — never chew or crush.
- Chewable tablets (Bonine, Bonine Max, Dramamine, Dramamine Chewable Orange, Meclizine HCL): Must be fully chewed or crushed before swallowing — never swallowed whole.
- Naus-ease film strips: Place on the tongue and let it dissolve completely, then swallow.
- Always follow your prescriber's instructions or the package directions. Do not take more than directed.
🤒Side effects — in detail▾
Most people taking meclizine experience mild side effects. The most commonly reported ones include:
- Drowsiness — the most frequent effect
- Dry mouth
- Headache
- Fatigue
- Vomiting
- Blurred vision (rare)
Rarely, a serious allergic reaction called anaphylaxis can occur — signs include hives, throat swelling, or difficulty breathing. Seek emergency medical help immediately if this happens.
⚠️Warnings & precautions▾
- Drowsiness: Meclizine commonly causes sleepiness. Avoid driving a car or operating dangerous machinery until you know how it affects you.
- Alcohol: Do not drink alcohol while taking meclizine — it significantly increases sedation.
- Asthma, glaucoma, or enlarged prostate: Meclizine's anticholinergic action may worsen these conditions. Use with caution and tell your doctor.
- Liver or kidney impairment: These conditions can slow how your body clears meclizine, leading to higher drug levels. Use cautiously.
- Older adults: Extra caution is needed, as kidney function naturally declines with age, which may cause the drug or its breakdown products to accumulate.
🔀What it interacts with▾
Meclizine can interact with several substances that affect how it works or amplify its side effects.
- Alcohol: Increases CNS (central nervous system) depression — can cause significant extra drowsiness and impaired coordination.
- Other CNS depressants (sleep medications, anti-anxiety drugs, opioid pain relievers, muscle relaxants): When combined with meclizine, these can cause additive sedation that may be unsafe.
- CYP2D6 inhibitors (certain antidepressants, some antifungals, and other drugs that inhibit this liver enzyme): Since meclizine is metabolized by the CYP2D6 enzyme, these drugs may raise meclizine levels in the blood, potentially increasing side effects. Tell your doctor and pharmacist about all medications you take.
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▾
- Allergy: Do not take meclizine if you are allergic to it or to any inactive ingredients in the product.
- Asthma, glaucoma, or enlarged prostate: Tell your doctor — meclizine's anticholinergic effects can aggravate these conditions.
- Pregnancy: Human studies have not shown a clear increased risk of birth defects, but animal studies showed fetal harm at doses similar to those used in humans. Discuss the risks and benefits with your doctor before taking meclizine during pregnancy.
- Breastfeeding: It is not known whether meclizine passes into breast milk or how it might affect a nursing infant. Talk to your doctor before using.
- Children under 12: Safety and effectiveness have not been established. Most OTC labels instruct not to give meclizine to children under 12 without a doctor's direction.
- Older adults: Start at the lower end of the dosing range. Reduced kidney and liver function with age means the drug may stay in the body longer.
- Liver impairment: Meclizine is processed by the liver; impairment may increase drug exposure. Use with caution.
- Kidney impairment: Reduced kidney function may cause meclizine or its breakdown products to accumulate. Use with caution.
🔬Pharmacokinetics — how your body processes it▾
After taking meclizine by mouth, it is absorbed through the digestive tract, with blood levels typically peaking around 3 hours after a dose (range: 1.5 to 6 hours) for tablet forms. Meclizine has a plasma elimination half-life — the time it takes for half the drug to be cleared from the blood — of about 5 to 6 hours. It is primarily broken down in the liver by an enzyme called CYP2D6, which means that drugs affecting this enzyme can alter how much meclizine stays active in your system. How meclizine distributes throughout body tissues is not well characterized in humans.
📦How to store it▾
Store at 20° to 25°C (68° to 77°F) . Dispense in a tight, light-resistant container (USP).
📄 Written from Meclizine’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 Meclizine
46 supplements and herbal products have documented interactions with Meclizine in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 3
- Moderate · 32
- 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 Meclizine — the kind of thing our pharmacy team would talk through with you at the counter.
What is meclizine actually used for? ▾
When should I take it before traveling? ▾
Will meclizine make me drowsy? ▾
Can I take meclizine if I'm pregnant or breastfeeding? ▾
Are there any health conditions that make meclizine less safe for me? ▾
Does it matter which form of meclizine I use — chewable, tablet, or dissolving film? ▾
Is Meclizine available over the counter? ▾
When was Meclizine first available? ▾
Who makes Meclizine? ▾
💬 Answers drafted from Meclizine’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 Meclizine comes
Meclizine is available in 5 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
- Dramamine Less Drowsy and Dramamine Less Drowsy Meclizine Hydrochloride: prevention and treatment of nausea, vomiting, and dizziness from motion sickness
- Dramamine-N: prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness
- Meclizine HCL 12.5 mg: prevention and treatment of nausea, vomiting, or dizziness due to motion sickness
- Antivert tablets: treatment of vertigo associated with vestibular system disorders in adults
- Swallow tablets whole — do not chew or crush
- For motion sickness, take approximately one hour before travel begins
- Taken orally once daily or in divided doses depending on condition and clinical response, as directed by a doctor
- Meclizine HCL 12.5 mg: consult a doctor for uses beyond motion sickness
Chewable tablet
How this form is used
- Prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness
- Bonine and Bonine Max: for motion sickness prevention and treatment in adults and children 12 and older
- Dramamine Chewable Orange: for prevention and treatment of nausea, vomiting, and dizziness from motion sickness
- Meclizine HCL chewable: for prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
- Chew or crush tablets completely before swallowing — do not swallow chewable tablets whole
- Bonine and Bonine Max: take one hour before travel starts; adults and children 12 and over take 1 to 2 tablets once daily or as directed by a doctor
- Bonine Max: take only 1 chewable tablet once daily; do not take more than directed
- Meclizine HCL chewable: dosage should be taken one hour before travel; not for children under 12 unless directed by a doctor
Orally disintegrating tablet
How this form is used
- CVS Motion Sickness Fast Melting: prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
- Wal-Dram 2 Quick-Dissolving: prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
Dissolving oral film
How this form is used
- Naus-ease film strips: prevention and treatment of nausea and vomiting associated with motion sickness
- Naus-ease film strips: treatment of dizziness associated with motion sickness
- Naus-ease film strips: treatment of vertigo
- Naus-ease film strips: place a strip on the tongue and allow it to dissolve completely, then swallow
- Naus-ease film strips: take the first dose one hour before travel for motion sickness prevention
- Naus-ease film strips: may be repeated every 24 hours for the duration of the journey
- Naus-ease film strips: for adults and children 12 years and over
Oral powder
How this form is used
- Dramamine oral powder: prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness
📊 Meclizine across the U.S. market
How Meclizine 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 (13) — 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 Meclizine is used
A general measure of how commonly Meclizine 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 Meclizine 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 Meclizine prescribed? Of the 1,596 medications we measure, Meclizine ranks #194 by Medicaid prescriptions — more than 88% of them.
Utilization by Meclizine 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.
meclizine hydrochloride 25 MG Oral Tablet Most dispensed
Summed across the 23 of 270 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 995666
meclizine hydrochloride 12.5 MG Oral Tablet
Summed across the 19 of 168 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 995624
meclizine hydrochloride 25 MG Chewable Tablet
Summed across the 6 of 159 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 995632
meclizine hydrochloride 50 MG Oral Tablet
Summed across the 1 of 15 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 995686
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 Meclizine, 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 49 of 612 listed Meclizine NDCs with Medicaid activity.
🔍 Compare Meclizine products
A representative set of FDA-listed product records for Meclizine — 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 |
|---|---|---|---|---|
| 💊Dissolving oral film | ||||
| 25 mg | Oral | Sunascen Therapeutics LLC × 2 listings | OTC MONOGRAPH FINAL | View NDC → |
| 💊Oral powder | ||||
| 50 mg | Oral | Medtech Products Inc. | OTC MONOGRAPH DRUG | View NDC → |
| 💊Tablet | ||||
| 12.5 mg | Oral | A-S Medication Solutions | OTC MONOGRAPH FINAL | Find on DailyMed ↗ |
| 12.5 mg | Oral | A-S Medication Solutions | ANDA | Find on DailyMed ↗ |
| 25 mg | Oral | A-S Medication Solutions × 9 listings | ANDA | View NDC → |
| 25 mg | Oral | A-S Medication Solutions | OTC MONOGRAPH FINAL | Find on DailyMed ↗ |
| 25 mg | Oral | Acme United Corporation | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Acme United Corporation | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Advanced Rx LLC | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Advanced Rx of Tennessee, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 12.5 mg | Oral | Advance Pharmaceutical Inc. | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | American Health Packaging × 4 listings | ANDA | View NDC → |
| 25 mg | Oral | American Health Packaging × 4 listings | ANDA | View NDC → |
| 25 mg | Oral | Amerisource Bergen × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Amerisource Bergen | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Amneal Pharmaceuticals LLC × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | Amneal Pharmaceuticals LLC × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | Amneal Pharmaceuticals LLC × 3 listings | ANDA | View NDC → |
| 12.5 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 12.5 mg | Oral | ANI Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 25 mg | Oral | ANI Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 12.5 mg | Oral | Apnar Pharma Lp | OTC MONOGRAPH DRUG | View NDC → |
| 12.5 mg | Oral | Apnar Pharma Lp | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Apnar Pharma Lp × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Apnar Pharma Lp × 2 listings | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Army And Air Force Exchange Service × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Army And Air Force Exchange Service | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Asclemed USA, Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Asclemed USA, Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Asclemed USA, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Asclemed USA, Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 12.5 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 25 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 50 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 25 mg | Oral | AvKARE × 2 listings | ANDA | View NDC → |
| 12.5 mg | Oral | AvPAK × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | AvPAK × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | Bell Pharmaceuticals, Inc. | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Bell Pharmaceuticals, Inc. | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Better Living Brands, LLC × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Better Living Brands, LLC | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | BluePoint Laboratories | OTC MONOGRAPH DRUG | View NDC → |
| 12.5 mg | Oral | BluePoint Laboratories | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Bryant Ranch Prepack × 13 listings | ANDA | View NDC → |
| 12.5 mg | Oral | Bryant Ranch Prepack × 4 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 12.5 mg | Oral | Bryant Ranch Prepack | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Bryant Ranch Prepack | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Bryant Ranch Prepack × 4 listings | ANDA | View NDC → |
| 25 mg | Oral | Bryant Ranch Prepack × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Bryant Ranch Prepack | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Cadila Healthcare Limited | ANDA | View NDC → |
| 25 mg | Oral | Cadila Healthcare Limited | ANDA | View NDC → |
| 25 mg | Oral | Cardinal Health 110, LLC. DBA Leader × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Cardinal Health 110, LLC. DBA Leader | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Casper Pharma LLC | NDA | View NDC → |
| 25 mg | Oral | Casper Pharma LLC | NDA | View NDC → |
| 50 mg | Oral | Casper Pharma LLC | NDA | View NDC → |
| 25 mg | Oral | Coupler LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Cvs Pharmacy × 2 listings | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | CVS Pharmacy, Inc | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | CVS Pharmacy, Inc × 2 listings | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Denton Pharma, Inc. dba Northwind Pharmaceuticals | ANDA | Find on DailyMed ↗ |
| 25 mg | Oral | Denton Pharma, Inc. DBA Northwind Pharmaceuticals × 5 listings | ANDA | View NDC → |
| 12.5 mg | Oral | Direct Rx | ANDA | Find on DailyMed ↗ |
| 12.5 mg | Oral | DirectRx × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Direct Rx × 2 listings | ANDA | View NDC → |
| 12.5 mg | Oral | Direct_Rx × 2 listings | ANDA | View NDC → |
| 25 mg | Oral | Direct_Rx × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Direct_Rx × 3 listings | ANDA | Find on DailyMed ↗ |
| 25 mg | Oral | Discount Drug Mart | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Discount Drug Mart | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Doh Central Pharmacy | ANDA | View NDC → |
| 25 mg | Oral | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Dolgencorp, Llc × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Dolgencorp, Llc | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Drug Ocean LLC | OTC MONOGRAPH FINAL | View NDC → |
| 12.5 mg | Oral | Drug Ocean LLC | OTC MONOGRAPH DRUG | View NDC → |
| 12.5 mg | Oral | Epic Pharma LLC | ANDA | View NDC → |
| 25 mg | Oral | Epic Pharma LLC | ANDA | View NDC → |
| 25 mg | Oral | Family Dollar Services Inc × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Family Dollar Services Inc | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Geiss, Destin & Dunn Inc. | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Geri-Care Pharmaceutical Corp | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Geri-Care Pharmaceutical Corp × 2 listings | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Golden State Medical Supply, Inc. × 2 listings | ANDA | View NDC → |
| 25 mg | Oral | Good Sense (Geiss, Destin & Dunn, Inc.) | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | H E B × 3 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | H E B | OTC MONOGRAPH FINAL | View NDC → |
| 50 mg | Oral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | JC World Bell Wholesale Co., Inc. | OTC MONOGRAPH DRUG | View NDC → |
| 12.5 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | Jubilant Cadista Pharmaceuticals Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Jubilant Cadista Pharmacuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | Jubilant Cadista Pharmacuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | Kroger Company × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | Kroger Company | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | L.N.K. International, Inc. × 3 listings | OTC MONOGRAPH DRUG | View NDC → |
| 25 mg | Oral | L.N.K. International, Inc. | OTC MONOGRAPH FINAL | View NDC → |
| 25 mg | Oral | Lake Erie Medical DBA Quality Care Products LLC | ANDA | View NDC → |
| 12.5 mg | Oral | Major Pharmaceuticals × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | Major Pharmaceuticals × 3 listings | ANDA | View NDC → |
| 25 mg | Oral | Medtech Products Inc. × 2 listings | OTC MONOGRAPH DRUG | View NDC → |
| 💊Bulk drug substance | ||||
| 1 kg/kg | — | Calyx Chemicals & Pharmaceuticals | BULK INGREDIENT | View NDC → |
| 1 mg/mg | — | Cohance Lifesciences Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Jubilant Biosys limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Professional Compounding Centers of America | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 1 kg/kg | — | R.L.Fine Chem Private Limited | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Spectrum Laboratory Products, Inc. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Srikem Laboratories Pvt. Ltd. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Sri Krishna Pharmaceuticals Ltd. Unit I | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Symed Labs Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | THINQ Pharma-CRO Limited | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Viyash Scientific Limited | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Xenex Laboratories Inc × 2 listings | BULK INGREDIENT | View NDC → |
Showing 200 of 505 products — FDA National Drug Code Directory. See every product, package size and price: browse all 505 Meclizine 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 Meclizine — 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 Meclizine 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 Meclizine 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 6676 5 dose forms · 9 strengths
-
Dose form (SCDF) Chewable Tablet RxCUI 372730In current FDA listings -
Dose form (SCDF) Disintegrating Oral Tablet RxCUI 1663814In current FDA listingsClinical drug / strength (SCD) hydrochloride 25 MGRxCUI 1663815 -
Dose form (SCDF) Oral Lozenge RxCUI 402352No current FDA listingClinical drug / strength (SCD) hydrochloride 12.5 MGRxCUI 995753 -
Dose form (SCDF) Oral Powder RxCUI 2734129In current FDA listingsClinical drug / strength (SCD) hydrochloride 50 MGRxCUI 2734132 -
Dose form (SCDF) Oral Tablet RxCUI 372731In current FDA listingsClinical drug / strength (SCD) hydrochloride 12.5 MGRxCUI 995624hydrochloride 25 MGRxCUI 995666hydrochloride 30 MGRxCUI 995682hydrochloride 50 MGRxCUI 995686
Look up RxCUI 6676 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 Meclizine 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 16 more on the FDA NDC directory.
RxNorm drug class
Meclizine belongs to the Antiemetic 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 163 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. Aurobindo Pharma Limited 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.