Methylphenidate
Methylphenidate is a CNS stimulant used to treat Attention Deficit Hyperactivity Disorder (ADHD) across multiple formulations, and certain products are also indicated for narcolepsy.
🧬 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 94 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 →
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Methylphenidate has a high potential for abuse, misuse, and addiction. Like other CNS stimulants, it can be misused — taken in higher doses than prescribed or by routes it's not meant for (such as snorting or injection). This dramatically increases the risk of overdose and death. Before starting this medication, your prescriber should assess your personal risk for misuse. Store it safely — ideally locked away — and never share it with anyone else. Dispose of any unused medication properly. Throughout treatment, watch for signs of misuse or dependence and discuss any concerns openly with your healthcare provider.
📖 Methylphenidate: Patient Information Guide
A plain-language walkthrough of Methylphenidate — 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▾
Methylphenidate is a CNS stimulant approved to treat ADHD and, in some formulations, narcolepsy. Specific approvals vary by product and age group:
- ADHD (ages 6 and older): Most formulations — including oral extended-release tablets (e.g., Concerta, Relexxii), extended-release capsules, oral solution, and chewable tablets — are approved for children 6 and up, adolescents, and (for some products) adults up to age 65.
- ADHD in children 6–12 only: Ritalin LA (extended-release capsules), methylphenidate hydrochloride extended-release capsules (LA and standard), and methylphenidate HCl Extended-Release Capsules CD are approved specifically for children ages 6 to 12 (CD approved to age 15).
- ADHD in patients 6–17 only: Cotempla XR-ODT (orally disintegrating tablet), methylphenidate extended-release orally disintegrating tablets, and the methylphenidate transdermal patch (Daytrana) are approved for pediatric patients ages 6 to 17.
- ADHD in adults up to age 65: Relexxii and certain extended-release tablet formulations are approved for adults up to 65 years of age.
- ADHD in patients 6 and older (including adults, no upper age specified): Jornay PM is approved for patients 6 years and older.
- Narcolepsy: Some methylphenidate hydrochloride extended-release tablet formulations and the oral solution and chewable tablets are also indicated for narcolepsy.
- Not recommended under age 6 for any formulation due to greater drug exposure and higher risk of side effects in that age group.
⚙️How it works▾
Methylphenidate works by blocking the reuptake of dopamine and norepinephrine — two key brain chemicals involved in attention, focus, and impulse control — back into the nerve cells that released them. It also increases the release of these chemicals into the space between nerve cells. The result is higher levels of both in the brain, which helps sharpen attention and reduce impulsivity and hyperactivity. Exactly why this helps ADHD is not fully understood, but the effect on these chemical pathways is thought to be central to its benefit.
Methylphenidate is a mixture of two forms (d- and l-isomers); the d-form is the more pharmacologically active one. It does not appear to significantly affect the heart's electrical rhythm at therapeutic doses, based on available data from studies of its active component.
💊How it's taken▾
The right way to take methylphenidate depends on which formulation is prescribed — they are not interchangeable on a milligram-for-milligram basis.
- Most oral extended-release tablets and capsules: Taken once daily in the morning, with or without food. Tablets must be swallowed whole. Some capsules may be opened and sprinkled on applesauce, but never chewed or crushed.
- Jornay PM (evening capsule): Uniquely taken in the evening — between 6:30 and 9:30 p.m. — consistently either with or without food. Can be sprinkled on applesauce.
- Oral liquid (Quillivant XR suspension): Taken once daily in the morning; shake the bottle vigorously for at least 10 seconds before each dose. May be taken with or without food.
- Transdermal patch (Daytrana): Applied to the hip (alternating sides) about 2 hours before the effect is needed, and removed 9 hours after application. Avoid applying external heat (heating pads, electric blankets) to the patch site.
Always follow your prescriber's instructions. Do not stop suddenly without talking to your doctor first, and never substitute one methylphenidate product for another without guidance.
🤒Side effects — in detail▾
The most common side effects vary a little between children and adults, but generally include:
- Decreased appetite and weight loss
- Trouble sleeping or initial insomnia
- Headache
- Nausea, stomach pain, or dry mouth
- Increased heart rate or palpitations
- Anxiety, irritability, or nervousness
- Dizziness
- Increased sweating
Seek prompt medical attention for more serious reactions: chest pain or fainting, new psychiatric symptoms (hallucinations, mania), prolonged or painful erections, numbness or color changes in fingers or toes, skin pigmentation loss (with the patch), or seizures. These are uncommon but require immediate evaluation.
⚠️Warnings & precautions▾
- Abuse, misuse, and addiction: Methylphenidate is a controlled substance with a real potential for abuse. Misuse — especially snorting or injection — can cause overdose and death. Store it securely and never share it.
- Heart risks: Avoid in anyone with structural heart defects, serious arrhythmias, coronary artery disease, or other serious cardiac conditions. Sudden death has been reported in such patients. Blood pressure and heart rate should be monitored regularly.
- Psychiatric effects: Can trigger or worsen hallucinations, mania, aggression, or paranoia — even in people with no prior psychiatric history. Screen for bipolar disorder before starting.
- Growth in children: Long-term use may temporarily slow height and weight gain in children. Doctors should monitor growth regularly.
- Priapism: Prolonged, painful erections have been reported. Seek immediate medical help if this occurs.
- Seizures: Stimulants may lower the seizure threshold. Discontinue if seizures occur.
- Circulation problems: Peripheral vasculopathy, including Raynaud's phenomenon (pain and color changes in fingers/toes), has been reported. Tell your doctor if you notice these changes.
- Patch-specific: The transdermal patch may cause permanent skin pigmentation loss (chemical leukoderma) or contact sensitization (skin allergy). Discontinue and contact your doctor if either occurs.
🔀What it interacts with▾
Methylphenidate has several important drug interactions to be aware of:
- MAO inhibitors (MAOIs): Absolutely contraindicated together or within 14 days of each other — the combination can cause hypertensive crisis (a dangerous, potentially fatal spike in blood pressure).
- Blood pressure medications: Methylphenidate can blunt their effectiveness; your doctor may need to adjust your antihypertensive dose and will monitor your blood pressure more closely.
- Halogenated anesthetics (surgery): Do not take methylphenidate on the day of surgery involving these anesthetics — the combination can cause sudden dangerous spikes in blood pressure and heart rate.
- Risperidone: Combining these medications may increase the risk of extrapyramidal symptoms (involuntary muscle movements or stiffness), especially when doses are changed.
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▾
- Do not take if you are allergic to methylphenidate or any ingredients in the specific product.
- Do not take if you are currently using or have used an MAOI within the past 14 days.
- Tell your doctor about any heart disease, high blood pressure, irregular heartbeat, or a family history of sudden cardiac death.
- Tell your doctor if you or a family member has a history of tics or Tourette's syndrome.
- Tell your doctor about any personal or family history of bipolar disorder, depression, or psychosis.
- Tell your doctor about any history of seizures or epilepsy.
- Not recommended in children under 6 years of age.
- Safety and effectiveness in adults over 65 has not been established.
- If you are pregnant: The data on risks to the fetus are inconsistent; there is a pregnancy registry you can join (1-866-961-2388). Discuss the risks and benefits with your doctor.
- If you are breastfeeding: Methylphenidate does pass into breast milk. Infants should be monitored for agitation, poor sleep, poor appetite, or slow weight gain. Discuss with your doctor.
🚑If you take too much▾
Taking too much methylphenidate can cause serious symptoms including rapid or irregular heartbeat, dangerously high blood pressure, agitation, confusion, hallucinations, seizures, and life-threatening high body temperature. In severe cases, it can lead to coma, stroke, or cardiac events. If an overdose is suspected, call the Poison Help line at 1-800-222-1222 or go to the nearest emergency room immediately — and if a patch was involved, remove it right away and clean the skin, as the drug can continue to absorb even after the patch is taken off.
📡Pharmacodynamics — effects in the body▾
Methylphenidate raises the levels of dopamine and norepinephrine between nerve cells by blocking their reuptake and increasing their release. This stimulates the central nervous system, improving attention and reducing impulsivity. It also increases heart rate and blood pressure modestly — on average, by a few beats per minute and a few mmHg — though some individuals may see larger increases. At therapeutic doses, it does not appear to cause meaningful changes in the heart's electrical rhythm (QT interval).
🔬Pharmacokinetics — how your body processes it▾
Methylphenidate is absorbed fairly quickly after oral dosing, though the timing and shape of drug levels in the blood depend on the formulation. Extended-release oral formulations are designed to deliver the drug in a more gradual, sustained way compared to immediate-release forms — some produce two distinct peaks of drug levels throughout the day. The drug's half-life (how long it takes the body to clear half of it) is approximately 3.5 hours in adults and adolescents. Methylphenidate is broken down mainly in the liver into an inactive metabolite and eliminated through the urine. It does not significantly accumulate in the body with once-daily dosing.
📦How to store it▾
Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) . Protect from humidity.
📄 Written from Methylphenidate’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 Methylphenidate
85 supplements and herbal products have documented interactions with Methylphenidate in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 6
- Moderate · 64
- Minor · 15
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 Methylphenidate — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is methylphenidate supposed to do for my ADHD? ▾
Will I get addicted to this medication? ▾
What side effects should I actually expect, and which ones mean I need to call my doctor? ▾
I take a medication for blood pressure. Is that a problem? ▾
Can I take this if I'm pregnant or breastfeeding? ▾
My child is on the skin patch — are there any special things I need to know? ▾
Is Methylphenidate available over the counter? ▾
Is Methylphenidate a controlled substance? ▾
When was Methylphenidate first available? ▾
Who makes Methylphenidate? ▾
💬 Answers drafted from Methylphenidate’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 Methylphenidate comes
Methylphenidate is available in 10 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.
Extended-release capsule
Extended-release tablet
Tablet
Show 1 more strength Show fewer strengths
Oral solution
Chewable tablet
Skin patch
Show 7 more strengths Show fewer strengths
Capsule
Extended-release chewable tablet
Orally disintegrating tablet
Extended-release oral suspension
📊 Methylphenidate across the U.S. market
How Methylphenidate 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 (25) — 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 Methylphenidate is used
A general measure of how commonly Methylphenidate 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 Methylphenidate 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 Methylphenidate prescribed? Of the 1,594 medications we measure, Methylphenidate ranks #35 by Medicaid prescriptions — more than 98% of them.
Utilization by Methylphenidate 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.
24 HR methylphenidate hydrochloride 36 MG Extended Release Oral Tablet Most dispensed
Summed across the 9 of 24 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091185
24 HR methylphenidate hydrochloride 27 MG Extended Release Oral Tablet
Summed across the 6 of 25 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091170
24 HR methylphenidate hydrochloride 18 MG Extended Release Oral Tablet
Summed across the 6 of 27 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091155
methylphenidate hydrochloride 10 MG Oral Tablet
Summed across the 10 of 40 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091150
24 HR methylphenidate hydrochloride 54 MG Extended Release Oral Tablet
Summed across the 6 of 25 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091210
methylphenidate hydrochloride 5 MG Oral Tablet
Summed across the 10 of 38 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091497
methylphenidate hydrochloride 20 MG Oral Tablet
Summed across the 11 of 44 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091392
24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension
Summed across the 4 of 4 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1312583
24 HR methylphenidate hydrochloride 20 MG Chewable Extended Release Oral Tablet
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1727443
30/70 Release 24 HR methylphenidate hydrochloride 20 MG Extended Release Oral Capsule
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806187
8 HR methylphenidate hydrochloride 20 MG Extended Release Oral Tablet
Summed across the 3 of 9 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091225
30/70 Release 24 HR methylphenidate hydrochloride 10 MG Extended Release Oral Capsule
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806181
methylphenidate hydrochloride 1 MG/ML Oral Solution
Summed across the 4 of 19 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091341
50/50 Release 24 HR methylphenidate hydrochloride 20 MG Extended Release Oral Capsule
Summed across the 5 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806177
Evening Dosing 24 HR methylphenidate hydrochloride 60 MG Extended Release Oral Capsule
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2168857
24 HR methylphenidate hydrochloride 30 MG Chewable Extended Release Oral Tablet
Summed across the 1 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1734928
Evening Dosing 24 HR methylphenidate hydrochloride 40 MG Extended Release Oral Capsule
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2168868
8 HR methylphenidate hydrochloride 10 MG Extended Release Oral Tablet
Summed across the 3 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091145
30/70 Release 24 HR methylphenidate hydrochloride 30 MG Extended Release Oral Capsule
Summed across the 4 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806189
Evening Dosing 24 HR methylphenidate hydrochloride 80 MG Extended Release Oral Capsule
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2168861
50/50 Release 24 HR methylphenidate hydrochloride 30 MG Extended Release Oral Capsule
Summed across the 6 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806179
30/70 Release 24 HR methylphenidate hydrochloride 40 MG Extended Release Oral Capsule
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806191
50/50 Release 24 HR methylphenidate hydrochloride 10 MG Extended Release Oral Capsule
Summed across the 5 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806195
BX Rating 24 HR methylphenidate hydrochloride 18 MG Extended Release Oral Tablet
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2001564
24 HR methylphenidate hydrochloride 40 MG Chewable Extended Release Oral Tablet
Summed across the 1 of 8 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1734951
Evening Dosing 24 HR methylphenidate hydrochloride 20 MG Extended Release Oral Capsule
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2168866
BX Rating 24 HR methylphenidate hydrochloride 27 MG Extended Release Oral Tablet
Summed across the 2 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2001565
Evening Dosing 24 HR methylphenidate hydrochloride 100 MG Extended Release Oral Capsule
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2168864
methylphenidate hydrochloride 2 MG/ML Oral Solution
Summed across the 4 of 17 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091133
BX Rating 24 HR methylphenidate hydrochloride 36 MG Extended Release Oral Tablet
Summed across the 2 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2001566
50/50 Release 24 HR methylphenidate hydrochloride 40 MG Extended Release Oral Capsule
Summed across the 6 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806183
BX Rating 24 HR methylphenidate hydrochloride 54 MG Extended Release Oral Tablet
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2001568
30/70 Release 24 HR methylphenidate hydrochloride 50 MG Extended Release Oral Capsule
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806193
methylphenidate hydrochloride 5 MG Chewable Tablet
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091322
30/70 Release 24 HR methylphenidate hydrochloride 60 MG Extended Release Oral Capsule
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806197
24 HR methylphenidate hydrochloride 72 MG Extended Release Oral Tablet
Summed across the 4 of 8 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1995461
methylphenidate hydrochloride 10 MG Chewable Tablet
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091152
methylphenidate hydrochloride 2.5 MG Chewable Tablet
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1091389
24 HR methylphenidate hydrochloride 45 MG Extended Release Oral Tablet
Summed across the 2 of 4 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2605798
methylphenidate 25.9 MG Disintegrating Oral Tablet
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1926849
methylphenidate 17.3 MG Disintegrating Oral Tablet
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1926840
9 HR methylphenidate 1.11 MG/HR Transdermal System
Summed across the 3 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 753436
9 HR methylphenidate 1.67 MG/HR Transdermal System
Summed across the 3 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 753438
9 HR methylphenidate 2.22 MG/HR Transdermal System
Summed across the 3 of 7 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 753440
methylphenidate 8.6 MG Disintegrating Oral Tablet
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1926853
40/60 Release 24 HR methylphenidate hydrochloride 50 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806204
24 HR methylphenidate hydrochloride 63 MG Extended Release Oral Tablet
Summed across the 2 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2605796
9 HR methylphenidate 3.33 MG/HR Transdermal System
Summed across the 3 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 753441
40/60 Release 24 HR methylphenidate hydrochloride 30 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806206
50/50 Release 24 HR methylphenidate hydrochloride 60 MG Extended Release Oral Capsule
Summed across the 2 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806185
40/60 Release 24 HR methylphenidate hydrochloride 40 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806210
40/60 Release 24 HR methylphenidate hydrochloride 20 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806202
40/60 Release 24 HR methylphenidate hydrochloride 15 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1648183
40/60 Release 24 HR methylphenidate hydrochloride 10 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806200
40/60 Release 24 HR methylphenidate hydrochloride 60 MG Extended Release Oral Capsule
Summed across the 2 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1806208
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 Methylphenidate, 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 177 of 448 listed Methylphenidate NDCs with Medicaid activity.
🔍 Compare Methylphenidate products
A representative set of FDA-listed product records for Methylphenidate — 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 |
|---|---|---|---|---|
| 💊Capsule | ||||
| 40 mg | — | Catalent Pharma Solutions, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 60 mg | — | Catalent Pharma Solutions, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 20 mg | Oral | Ironshore Pharmaceuticals Inc. × 3 listings | NDA | View NDC → |
| 40 mg | Oral | Ironshore Pharmaceuticals Inc. × 3 listings | NDA | View NDC → |
| 60 mg | Oral | Ironshore Pharmaceuticals Inc. × 3 listings | NDA | View NDC → |
| 80 mg | Oral | Ironshore Pharmaceuticals Inc. × 3 listings | NDA | View NDC → |
| 100 mg | Oral | Ironshore Pharmaceuticals Inc. × 3 listings | NDA | View NDC → |
| 10 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 20 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 30 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 40 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 50 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 60 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 💊Extended-release capsule | ||||
| 10 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 15 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 20 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 30 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 40 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 50 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 60 mg | Oral | Actavis Pharma, Inc. × 2 listings | ANDA | View NDC → |
| 25 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 35 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 45 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 55 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 70 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 85 mg | Oral | Adlon Therapeutics L.P. | NDA | View NDC → |
| 10 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 20 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 30 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 40 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 60 mg | Oral | Amneal Pharmaceuticals of New York LLC × 3 listings | ANDA | View NDC → |
| 10 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 20 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 30 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 40 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 50 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 60 mg | Oral | Aytu BioPharma, Inc. | NDA | View NDC → |
| 10 mg | — | Catalent Pharma Solutions, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 20 mg | — | Catalent Pharma Solutions, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 30 mg | — | Catalent Pharma Solutions, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 20 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 40 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 60 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 80 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 100 mg | — | Coating Place, LLC | DRUG FOR FURTHER PROCESSING | View NDC → |
| 10 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 20 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 30 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 40 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 60 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 10 mg | Oral | Granules Pharmaceuticals Inc. × 3 listings | ANDA | View NDC → |
| 20 mg | Oral | Granules Pharmaceuticals Inc. × 3 listings | ANDA | View NDC → |
| 30 mg | Oral | Granules Pharmaceuticals Inc. × 3 listings | ANDA | View NDC → |
| 40 mg | Oral | Granules Pharmaceuticals Inc. × 3 listings | ANDA | View NDC → |
| 60 mg | Oral | Granules Pharmaceuticals Inc. × 3 listings | ANDA | View NDC → |
| 10 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 20 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg | Oral | Lannett Company, Inc. × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 10 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 20 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 20 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 30 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 40 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 50 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg | Oral | Lannett Company, LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg | Oral | Lannett Company, LLC | NDA | View NDC → |
| 10 mg | Oral | Mayne Pharma × 2 listings | ANDA | View NDC → |
| 20 mg | Oral | Mayne Pharma × 2 listings | ANDA | View NDC → |
| 30 mg | Oral | Mayne Pharma × 4 listings | ANDA | View NDC → |
| 40 mg | Oral | Mayne Pharma × 4 listings | ANDA | View NDC → |
| 60 mg | Oral | Mayne Pharma × 2 listings | ANDA | View NDC → |
| 10 mg | Oral | Novartis Pharmaceuticals Corporation × 3 listings | NDA | View NDC → |
| 20 mg | Oral | Novartis Pharmaceuticals Corporation × 3 listings | NDA | View NDC → |
| 30 mg | Oral | Novartis Pharmaceuticals Corporation × 3 listings | NDA | View NDC → |
| 40 mg | Oral | Novartis Pharmaceuticals Corporation × 3 listings | NDA | View NDC → |
| 10 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 15 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 20 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg | Oral | Rhodes Pharmaceuticals × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 15 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 20 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg | Oral | Rhodes Pharmaceuticals LLC | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | Oral | Sandoz Inc × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 20 mg | Oral | Sandoz Inc × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg | Oral | Sandoz Inc × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg | Oral | Sandoz Inc × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 10 mg | — | Societal CDMO Gainesville, LLC × 4 listings | DRUG FOR FURTHER PROCESSING | View NDC → |
| 20 mg | — | Societal CDMO Gainesville, LLC × 4 listings | DRUG FOR FURTHER PROCESSING | View NDC → |
| 30 mg | — | Societal CDMO Gainesville, LLC × 4 listings | DRUG FOR FURTHER PROCESSING | View NDC → |
| 40 mg | — | Societal CDMO Gainesville, LLC × 4 listings | DRUG FOR FURTHER PROCESSING | View NDC → |
| 60 mg | — | Societal CDMO Gainesville, LLC × 2 listings | DRUG FOR FURTHER PROCESSING | View NDC → |
| 20 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 30 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 40 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 50 mg | Oral | SpecGx LLC | ANDA | View NDC → |
Showing 200 of 746 products — FDA National Drug Code Directory. See every product, package size and price: browse all 746 Methylphenidate 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 Methylphenidate — 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 Methylphenidate 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 Methylphenidate 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 6901 9 dose forms · 56 strengths
-
Dose form (SCDF) Chewable Extended Release Oral Tablet RxCUI 2270756In current FDA listingsClinical drug / strength (SCD) 24 HR methylphenidate hydrochloride 20 MGRxCUI 172744324 HR methylphenidate hydrochloride 30 MGRxCUI 173492824 HR methylphenidate hydrochloride 40 MGRxCUI 1734951 -
Dose form (SCDF) Chewable Tablet RxCUI 476365In current FDA listingsClinical drug / strength (SCD) hydrochloride 10 MGRxCUI 1091152hydrochloride 2.5 MGRxCUI 1091389hydrochloride 5 MGRxCUI 1091322 -
Dose form (SCDF) Disintegrating Oral Tablet RxCUI 1926839In current FDA listings -
Dose form (SCDF) Extended Release Oral Capsule RxCUI 374655In current FDA listingsClinical drug / strength (SCD) Evening Dosing 24 HR methylphenidate hydrochloride 100 MGRxCUI 2168864Evening Dosing 24 HR methylphenidate hydrochloride 20 MGRxCUI 2168866Evening Dosing 24 HR methylphenidate hydrochloride 40 MGRxCUI 2168868Evening Dosing 24 HR methylphenidate hydrochloride 60 MGRxCUI 2168857Evening Dosing 24 HR methylphenidate hydrochloride 80 MGRxCUI 216886130/70 Release 24 HR methylphenidate hydrochloride 10 MGRxCUI 180618130/70 Release 24 HR methylphenidate hydrochloride 20 MGRxCUI 180618730/70 Release 24 HR methylphenidate hydrochloride 30 MGRxCUI 180618930/70 Release 24 HR methylphenidate hydrochloride 40 MGRxCUI 180619130/70 Release 24 HR methylphenidate hydrochloride 50 MGRxCUI 180619330/70 Release 24 HR methylphenidate hydrochloride 60 MGRxCUI 180619740/60 Release 24 HR methylphenidate hydrochloride 10 MGRxCUI 180620040/60 Release 24 HR methylphenidate hydrochloride 15 MGRxCUI 164818340/60 Release 24 HR methylphenidate hydrochloride 20 MGRxCUI 180620240/60 Release 24 HR methylphenidate hydrochloride 30 MGRxCUI 180620640/60 Release 24 HR methylphenidate hydrochloride 40 MGRxCUI 180621040/60 Release 24 HR methylphenidate hydrochloride 50 MGRxCUI 180620440/60 Release 24 HR methylphenidate hydrochloride 60 MGRxCUI 180620850/50 Release 24 HR methylphenidate hydrochloride 10 MGRxCUI 180619550/50 Release 24 HR methylphenidate hydrochloride 20 MGRxCUI 180617750/50 Release 24 HR methylphenidate hydrochloride 30 MGRxCUI 180617950/50 Release 24 HR methylphenidate hydrochloride 40 MGRxCUI 180618350/50 Release 24 HR methylphenidate hydrochloride 60 MGRxCUI 1806185 -
Dose form (SCDF) Extended Release Oral Tablet RxCUI 372862In current FDA listingsClinical drug / strength (SCD) BX Rating 24 HR methylphenidate hydrochloride 18 MGRxCUI 2001564BX Rating 24 HR methylphenidate hydrochloride 27 MGRxCUI 2001565BX Rating 24 HR methylphenidate hydrochloride 36 MGRxCUI 2001566BX Rating 24 HR methylphenidate hydrochloride 54 MGRxCUI 20015688 HR methylphenidate hydrochloride 10 MGRxCUI 10911458 HR methylphenidate hydrochloride 20 MGRxCUI 109122524 HR methylphenidate hydrochloride 18 MGRxCUI 109115524 HR methylphenidate hydrochloride 27 MGRxCUI 109117024 HR methylphenidate hydrochloride 36 MGRxCUI 109118524 HR methylphenidate hydrochloride 45 MGRxCUI 260579824 HR methylphenidate hydrochloride 54 MGRxCUI 109121024 HR methylphenidate hydrochloride 63 MGRxCUI 260579624 HR methylphenidate hydrochloride 72 MGRxCUI 1995461 -
Dose form (SCDF) Extended Release Suspension RxCUI 1312582In current FDA listingsClinical drug / strength (SCD) 24 HR methylphenidate hydrochloride 5 MG/MLRxCUI 1312583 -
Dose form (SCDF) Oral Solution RxCUI 476368In current FDA listingsClinical drug / strength (SCD) hydrochloride 1 MG/MLRxCUI 1091341hydrochloride 2 MG/MLRxCUI 1091133 -
Dose form (SCDF) Oral Tablet RxCUI 372861In current FDA listingsClinical drug / strength (SCD) hydrochloride 10 MGRxCUI 1091150hydrochloride 2.5 MGRxCUI 1091501hydrochloride 20 MGRxCUI 1091392hydrochloride 5 MGRxCUI 1091497 -
Dose form (SCDF) Transdermal System RxCUI 1805912In current FDA listingsClinical drug / strength (SCD) 9 HR methylphenidate 1.11 MG/HRRxCUI 7534369 HR methylphenidate 1.67 MG/HRRxCUI 7534389 HR methylphenidate 2.22 MG/HRRxCUI 7534409 HR methylphenidate 3.33 MG/HRRxCUI 753441
Look up RxCUI 6901 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 Methylphenidate 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
Methylphenidate belongs to the Central Nervous System Stimulant 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 94 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. Sandoz Inc 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.