Amphetamine
Amphetamine is a CNS stimulant used across several products to treat ADHD, narcolepsy, and — in certain tablet formulations — short-term obesity management.
🧬 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 29 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 →
Amphetamine is a stimulant, a usual first choice for ADHD that is also approved in some tablet forms for narcolepsy and short-term weight loss; it works by making nerve cells release more dopamine and norepinephrine and reabsorb less, has been on the U.S. market since about 1999, and is available as a generic. Most people tolerate it well, though appetite loss, dry mouth, and trouble sleeping (worse with late doses) are common. Its boxed warning is for abuse, misuse and addiction, and it raises heart rate and blood pressure and can trigger psychiatric symptoms, so report chest pain, an irregular heartbeat, or hallucinations promptly.
Clinical pearls
- Vitamin C, fruit juice and some antacids can weaken its effect, while sodium bicarbonate can strengthen it.
- Avoid alcohol with the extended-release forms, since alcohol can make them release the medicine far too quickly.
- Never take it within 14 days of an MAO inhibitor antidepressant, and tell every prescriber about any other antidepressant.
- Children taking it should have height and weight checked regularly, because stimulants can slow growth over time.
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Amphetamine has a high potential for abuse, misuse, and addiction. Using it in ways other than prescribed — such as taking higher doses, snorting, or injecting — greatly raises the risk of overdose and death. Even when taken as prescribed, some people may develop a dependence or substance use disorder over time. Before starting, your prescriber should assess your personal risk. Store this medication in a secure, preferably locked place, do not share it with anyone, and safely dispose of any unused supply. If you notice signs of misuse — such as taking more than prescribed, craving the drug, or using it to get high — tell your doctor right away.
Patient information guide A plain-language walkthrough of Amphetamine, written from its FDA label.
What Amphetamine is used for
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Amphetamine is a CNS stimulant available in several products, each with its own approved uses:
- ADHD (Attention Deficit Hyperactivity Disorder): Adzenys XR-ODT, Dyanavel XR, Amphetamine Extended-Release orally disintegrating tablets, Amphetamine Sulfate tablets, and Evekeo are all approved for ADHD. The extended-release products are approved for patients 6 years and older; the extended-release forms are not recommended under age 6.
- Narcolepsy: Amphetamine Sulfate tablets and Evekeo are approved to treat narcolepsy (a condition causing uncontrollable daytime sleepiness).
- Exogenous obesity (short-term): Amphetamine Sulfate tablets and Evekeo may be used short-term as part of a calorie-restricted weight-loss program for people who have not responded to other weight-loss approaches.
How Amphetamine works
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Amphetamine works by increasing the availability of two key brain chemicals: dopamine and norepinephrine. It blocks their reabsorption into nerve cells and triggers a greater release of these chemicals into the gaps between nerves. This boosts communication along pathways that regulate attention, impulse control, and alertness. The exact way this improves ADHD symptoms is not fully known, but these effects on brain chemistry are thought to be central to how it helps.
Amphetamine dosage
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All amphetamine forms are taken by mouth. Most formulations are taken once daily in the morning to avoid interfering with sleep. Evekeo and Amphetamine Sulfate tablets may be taken in divided doses throughout the day, with the first dose on waking and additional doses spaced 4 to 6 hours apart — again, avoiding late evening doses.
- Most formulations can be taken with or without food; food may slightly delay onset but does not meaningfully change overall absorption.
- Dose is always individualized — your prescriber will start low and adjust based on how you respond.
- Different amphetamine products are not interchangeable milligram for milligram — never switch products without your prescriber's guidance.
Dosing details from the FDA-approved label
From the Amphetamine prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Pediatric patients (ages 6 to 17 years) - Amphetamine extended-release orally disintegrating tablets / Adzenys XR-ODT
- Starting dose is 6.3 mg once daily in the morning
- Increase in increments of 3.1 mg or 6.3 mg at weekly intervals
- Maximum: 18.8 mg once daily for patients 6 to 12 years, and 12.5 mg once daily for patients 13 to 17 years
- May be taken with or without food; allow tablet to disintegrate in saliva then swallow
- Adults - Amphetamine extended-release orally disintegrating tablets / Adzenys XR-ODT
- 12.5 mg once daily in the morning
- May be taken with or without food; allow tablet to disintegrate in saliva then swallow
- Switching from ADDERALL XR to amphetamine extended-release orally disintegrating tablets / Adzenys XR-ODT
- Switch at the equivalent dose taken once daily: 3.1 mg = 5 mg, 6.3 mg = 10 mg, 9.4 mg = 15 mg, 12.5 mg = 20 mg, 15.7 mg = 25 mg, 18.8 mg = 30 mg ADDERALL XR
- Do not substitute for other amphetamine products on a milligram-per-milligram basis; if switching from any other amphetamine product, discontinue it and titrate
- Dyanavel XR (oral suspension and extended-release tablets)
- Recommended starting dosage is 2.5 mg or 5 mg once daily in the morning
- May be increased in increments of 2.5 mg to 10 mg per day every 4 to 7 days
- Maximum: 20 mg daily
- May be taken with or without food; shake suspension before use; tablets may be chewed or swallowed whole; suspension can be substituted with tablets on a milligram per milligram basis
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION May be taken with or without food. Allow tablet to disintegrate in saliva then swallow. ( 2.2 ) Pediatric patients (ages 6 to 17 years): Starting dose is 6.3 mg once daily in the morning. Maximum dose is 18.8 mg once daily for patients 6 to 12 years, and 12.5 mg once daily for patients 13 to 17 years. ( 2.3 ) Adults: 12.5 mg once daily in the morning. ( 2.4 ) To avoid substitution errors and overdosage, do not substitute for other amphetamine products on a milligram-per-milligram basis because of different amphetamine base compositions and differing pharmacokinetic profiles. ( 2.5 , 5.7 ) 2.1 Pre-treatment Screening Prior to treating patients with amphetamine extended-release orally disintegrating tablets, assess: for the presence of cardiac disease (i.e., perform a careful history, family history of sudden death or ventricular arrhythmia, and physical exam) [see Warnings and Precautions ( 5.2 ) ] . the family history and clinically evaluate patients for motor or verbal tics or Tourette’s syndrome before initiating amphetamine extended-release orally disintegrating tablets [see Warnings and Precautions ( 5.9 )] . 2.2 General Administration Information Amphetamine extended-release orally disintegrating tablets may be taken orally with or without food. Individualize the dosage according to the therapeutic needs and response of the patient. Amphetamine extended-release orally disintegrating tablets should be taken as follows: The tablet should remain in the blister pack until the patient is ready to take it. The patient or caregiver should use dry hands to open the blister. Tear along the perforation, bend the blister where indicated and peel back the blister’s labeled backing to take out the tablet. The tablet should not be pushed through the foil. As soon as the blister is opened, the tablet should be removed and placed on the patient’s tongue. The whole tablet should be placed on the tongue and allowed to disintegrate without chewing or crushing. The tablet will disintegrate in saliva so that it can be swallowed. 2.3 Dosage Recommendations in Pediatric Patients The recommended starting dosage is 6.3 mg once daily in the morning. Increase in increments of 3.1 mg or 6.3 mg at weekly intervals.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Amphetamine side effects
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The most commonly reported side effects of amphetamine include:
Common side effects
- Loss of appetite
- Trouble sleeping (insomnia)
- Stomach pain or nausea
- Dry mouth
- Weight loss
- Headache
- Anxiety or nervousness
- Increased heart rate
- Stomach pain, nausea, or vomiting
- Dizziness
When to get medical help
- Call your doctor if you notice chest pain, irregular heartbeat, or shortness of breath
- Seek help right away for signs of serotonin syndrome: agitation, hallucinations, rapid heart rate, high fever, stiff muscles, or loss of coordination
- Tell your doctor if you develop new or worsening mood or behavior changes, hallucinations, or manic episodes
- Contact your doctor if you notice numbness, color changes, or sores in fingers or toes (signs of circulation problems)
- Get help immediately for signs of a severe allergic reaction: swelling of the face or throat, rash, or difficulty breathing
- Tell your doctor about unusual or worsening tics or Tourette's syndrome symptoms
- Seek emergency care for signs of overdose: dangerously high fever, seizures, confusion, or very high blood pressure
Serious reactions that need prompt medical attention include signs of serotonin syndrome (fever, muscle stiffness, rapid heart rate, confusion), new psychiatric symptoms (hallucinations, mania), circulation problems in fingers or toes, or signs of a severe allergic reaction such as facial swelling or difficulty breathing.
Amphetamine warnings and precautions
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- Abuse, misuse, and addiction: Amphetamine has a high potential for abuse. Misuse — especially snorting or injecting — can cause overdose and death. Store it securely, don't share it, and dispose of unused medication properly.
- Heart risks: Sudden death has occurred in patients with underlying heart conditions. People with structural heart defects, serious arrhythmia, or coronary artery disease should not take amphetamine. All patients should have blood pressure and heart rate monitored regularly.
- Psychiatric effects: Amphetamine can trigger or worsen hallucinations, mania, or psychosis — even in people with no prior psychiatric history. Screen for bipolar disorder before starting.
- Growth in children: Long-term use may slow height and weight gain in children. Pediatric patients should be monitored closely, and treatment may need to be paused if growth is affected.
- Serotonin syndrome: A potentially life-threatening reaction can occur when amphetamine is combined with certain antidepressants or other serotonergic drugs.
- Circulation problems: Raynaud's phenomenon (color changes, pain, or sores in fingers/toes) has been reported and should be watched for during treatment.
Amphetamine interactions
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Amphetamine interacts with a number of medications and substances — always give your pharmacist and prescriber a full list of everything you take:
- MAO inhibitors (MAOIs): Extremely dangerous combination — can cause hypertensive crisis (a sudden, severe spike in blood pressure) and potentially fatal neurological effects. Do not take within 14 days of an MAOI.
- Serotonergic drugs (SSRIs, SNRIs, triptans, tricyclic antidepressants, lithium, tramadol, St. John's Wort, buspirone, fentanyl, tryptophan): Increase the risk of serotonin syndrome when combined with amphetamine.
- CYP2D6 inhibitors (fluoxetine, paroxetine, quinidine, ritonavir): Can raise amphetamine blood levels, increasing both effects and side effect risk.
- Acidifying agents (vitamin C, fruit juices, certain medications): Lower absorption and reduce amphetamine's effectiveness.
- Alkalinizing agents (sodium bicarbonate, some diuretics): Increase amphetamine blood levels and may intensify its effects.
- Blood pressure medications: Amphetamine may reduce how well they work.
- Alcohol: High alcohol concentrations caused a large, rapid release of amphetamine from extended-release formulations in lab studies — avoid alcohol during treatment.
Interactions listed in the FDA-approved label
From the Amphetamine prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- MAO inhibitors (MAOI antidepressants, metabolite of furazolidone): Slow amphetamine metabolism, potentiating amphetamines; this can cause headaches and other signs of hypertensive crisis, neurological toxic effects and malignant hyperpyrexia, sometimes fatal.
- Serotonergic drugs: Concomitant use increases the risk of serotonin syndrome. Initiate with lower doses and monitor for serotonin syndrome, particularly at initiation or dosage increase; if it occurs, discontinue amphetamine and the serotonergic drug(s).
- CYP2D6 inhibitors (e.g., paroxetine, fluoxetine, quinidine, ritonavir): May increase amphetamine exposure and increase the risk of serotonin syndrome. Initiate with lower doses and monitor for serotonin syndrome at initiation and after a dosage increase; if it occurs, discontinue amphetamine and the CYP2D6 inhibitor.
- Acidifying agents (GI and urinary, e.g., ascorbic acid, fruit juices, ammonium chloride): Lower absorption and/or increase urinary excretion of amphetamines, lowering blood levels and efficacy. Adjust dosage accordingly.
- Alkalinizing agents (e.g., sodium bicarbonate, acetazolamide, some thiazides): Increase absorption and/or decrease urinary excretion of amphetamines, increasing blood levels and potentiating their action. Adjust dosage accordingly.
- Tricyclic antidepressants: Amphetamines may enhance their activity; d-amphetamine with desipramine or protriptyline causes striking and sustained increases in brain d-amphetamine concentration and cardiovascular effects can be potentiated.
- Adrenergic blockers: Adrenergic blockers are inhibited by amphetamines.
- Antihistamines: Amphetamines may counteract the sedative effect of antihistamines.
- Antihypertensives: Amphetamines may antagonize the hypotensive effects of antihypertensives.
- Chlorpromazine: Blocks dopamine and norepinephrine reuptake, inhibiting the central stimulant effects of amphetamine. Can be used to treat amphetamine poisoning.
Read the label’s full interactions text
Drug Interactions MAO inhibitors - MAOI antidepressants, as well as a metabolic of furazolidone, slow amphetamine metabolism. This slowing potentiates amphetamines, increasing their effect on the release of norepinephrine and other monoamines from adrenergic nerve endings; this can cause headaches and other signs of hypertensive crisis. A variety of neurological toxic effects and malignant hyperpyrexia can occur, sometimes with fatal results. Serotonergic drugs - The concomitant use of amphetamine sulfate tablets and serotonergic drugs increases the risk of serotonin syndrome. Initiate with lower doses and monitor patients for signs and symptoms of serotonin syndrome, particularly during amphetamine sulfate tablets initiation or dosage increase. If serotonin syndrome occurs, discontinue amphetamine sulfate tablets and the concomitant serotonergic drug(s) ( see WARNINGS and PRECAUTIONS ). CYP2D6 inhibitors - The concomitant use of amphetamine sulfate tablets and CYP2D6 inhibitors may increase the exposure of amphetamine sulfate tablets compared to the use of the drug alone and increase the risk of serotonin syndrome. Initiate with lower doses and monitor patients for signs and symptoms of serotonin syndrome particularly during amphetamine sulfate tablets initiation and after a dosage increase. If serotonin syndrome occurs, discontinue amphetamine sulfate tablets and the CYP2D6 inhibitor ( see WARNINGS and OVERDOSAGE ). Examples of CYP2D6 Inhibitors include paroxetine and fluoxetine (also serotonergic drugs), quinidine, ritonavir. Acidifying agents - Gastrointestinal acidifying agents (guanethidine, reserpine, glutamic acid HCl, ascorbic acid, fruit juices, etc.) lower absorption of amphetamines. Urinary acidifying agents (ammonium chloride, sodium acid phosphate, etc.) increase concentration of the ionized species of the amphetamine molecule, thereby increasing urinary excretion. Both groups of agents lower blood levels and efficacy of amphetamines.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Amphetamine
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- Tell your doctor if you have any heart disease, including irregular heartbeat, structural heart problems, or coronary artery disease — amphetamine is not safe for people with serious cardiac conditions.
- Share any personal or family history of bipolar disorder, depression, psychosis, or suicidal behavior.
- Mention any history of motor or verbal tics or Tourette's syndrome — amphetamine can worsen these.
- Tell your doctor if you are pregnant: amphetamine may cause premature delivery, low birth weight, and withdrawal symptoms in newborns.
- Breastfeeding is not recommended — amphetamine passes into breast milk and long-term effects on nursing infants are unknown.
- Extended-release amphetamine products are not recommended for children under 6 years old; Evekeo and Amphetamine Sulfate tablets have separate age-related dosing guidance.
- Tell your prescriber about all other medications, supplements, and herbal products you take — especially antidepressants, blood pressure drugs, and seizure medicines.
- Do not take amphetamine if you are allergic to it or any of its ingredients, or if you have taken an MAOI in the past 14 days.
Amphetamine overdose
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Taking too much amphetamine can cause a rapid or irregular heartbeat, dangerously high or low blood pressure, high fever, seizures, confusion, hallucinations, and in severe cases, heart attack, stroke, or coma. If you suspect an overdose, call 911 or the Poison Help line at 1-800-222-1222 right away. Amphetamine cannot be removed from the body with dialysis, so emergency supportive care is the primary treatment.
What Amphetamine does in the body
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Amphetamine increases blood pressure and heart rate — on average, blood pressure rises by about 2 to 4 mmHg and heart rate by about 3 to 6 beats per minute, though some people may see larger increases. It also suppresses appetite, can reduce the urge to sleep, and stimulates the central nervous system. These effects stem from its action on norepinephrine and dopamine pathways throughout the brain and body.
How your body processes Amphetamine
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After taking an extended-release orally disintegrating tablet, amphetamine reaches peak blood levels in about 5 hours on an empty stomach; food delays peak levels by roughly 2 hours but does not significantly change total absorption. The drug is broken down in the liver (partly through an enzyme called CYP2D6) and cleared mainly through the urine — and how much is excreted depends heavily on urine acidity. The half-life (time for half the drug to leave the body) is about 11 hours in adults for d-amphetamine and about 9 to 10 hours in children ages 6 to 12; l-amphetamine stays in the body somewhat longer.
How to store Amphetamine
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Store at 20°C to 25º C (68°F to 77º F). Store ADZENYS XR-ODT blister packages in the rigid, plastic travel case provided after removal from the carton.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Amphetamine
130 supplements and herbal products have documented interactions with Amphetamine in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 16
- Moderate · 97
- Minor · 17
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.
Amphetamine: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Amphetamine — the kind of thing our pharmacy team would talk through with you at the counter.
What conditions is amphetamine actually approved to treat?
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Is it okay to take this with food, or does it have to be on an empty stomach?
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What side effects should I actually expect, and what would make me call my doctor?
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I've heard this medication can be addictive. Should I be worried?
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Can my child take this, and are there any specific concerns for kids?
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Are there any medications I absolutely cannot take with amphetamine?
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Is Amphetamine available over the counter?
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Is Amphetamine a controlled substance?
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When was Amphetamine first available?
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Who makes Amphetamine?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Amphetamine on HelloPharmacist
Amphetamine forms and strengths (how it comes)
Amphetamine is available in 4 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
- Amphetamine Sulfate tablets and Evekeo are approved for ADHD as part of a broader treatment program including psychological and educational support
- Amphetamine Sulfate tablets and Evekeo are approved for narcolepsy
- Evekeo is approved as a short-term aid in a calorie-restricted weight-loss program for exogenous obesity in patients who have not responded to other treatments
- Amphetamine Sulfate tablets are approved for exogenous obesity as a short-term adjunct to caloric restriction
- Evekeo and Amphetamine Sulfate tablets are taken by mouth; the first dose is given on awakening, with any additional doses spaced 4 to 6 hours apart
- Late evening doses should be avoided to prevent insomnia
- Dose is adjusted individually based on response and tolerability — always follow your prescriber's guidance
Orally disintegrating tablet
How this form is used
- Adzenys XR-ODT is approved for the treatment of ADHD in patients 6 years and older
- Amphetamine Extended-Release orally disintegrating tablets are approved for ADHD in patients 6 years and older
- These extended-release orally disintegrating formulations are not recommended in children under 6 years of age
- Adzenys XR-ODT and amphetamine extended-release orally disintegrating tablets should be kept in the blister pack until ready to use — open with dry hands, peel back the backing, and place the tablet on the tongue to dissolve, then swallow
- These orally disintegrating tablets may be taken with or without food
- Take once daily in the morning; do not substitute for other amphetamine products on a mg-per-mg basis
Show 4 more strengths Show fewer strengths
Extended-release tablet
How this form is used
- Dyanavel XR extended-release tablets are approved to treat ADHD in patients 6 years and older
- Dyanavel XR is not recommended for children under 6 years of age
- Dyanavel XR extended-release tablets may be chewed or swallowed whole
- Dyanavel XR tablets are taken once daily in the morning, with or without food
- Do not substitute Dyanavel XR for other amphetamine products on a mg-per-mg basis due to different formulations and absorption profiles
Extended-release oral suspension
How this form is used
- Dyanavel XR is approved to treat ADHD in patients 6 years and older
- Dyanavel XR is not recommended for children under 6 years of age
- Dyanavel XR oral suspension should be shaken well before each dose
- Dyanavel XR is taken once daily in the morning, with or without food
- Dyanavel XR oral suspension can be switched to Dyanavel XR tablets milligram for milligram, but do not substitute for other amphetamine products on a mg-per-mg basis
Amphetamine on the U.S. market: products, makers and brands
How Amphetamine 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.
16 companies list 58 Amphetamine product records with the FDA, mostly as tablet, orally disintegrating tablet, extended-release tablet; the earliest marketing or approval year on record is 1955. Brand names on the directory include Adzenys ER, Adzenys XR, Dyanavel XR and 5 more; the rest are generics.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (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 Amphetamine is used (Medicaid data)
A general measure of how commonly Amphetamine 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 Amphetamine 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 Amphetamine prescribed? Of the 1,601 medications we measure, Amphetamine ranks #521 by Medicaid prescriptions — more than 67% of them.
Utilization by Amphetamine 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 amphetamine 2.5 MG/ML Extended Release Suspension Most dispensed
Summed across the 1 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1720586
24 HR amphetamine 20 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 2585468
24 HR amphetamine 10 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 2585460
24 HR amphetamine 15 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 2585462
24 HR amphetamine 5 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 2585473
24 HR amphetamine 18.8 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 1739819
24 HR amphetamine 12.5 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 1739803
24 HR amphetamine 15.7 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 1739813
24 HR amphetamine 9.4 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 1739837
amphetamine sulfate 10 MG Oral Tablet
Summed across the 4 of 24 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1600695
24 HR amphetamine 6.3 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 1739831
amphetamine sulfate 5 MG Oral Tablet
Summed across the 4 of 23 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 884655
24 HR amphetamine 3.1 MG Extended Release Oral Tablet
Summed across the 1 of 4 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1739825
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 Amphetamine, 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 24 of 78 listed Amphetamine NDCs with Medicaid activity.
Compare Amphetamine products
A representative set of FDA-listed product records for Amphetamine — 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 |
|---|---|---|---|---|
| 💊Extended-release oral suspension | ||||
| 2.5 mg/mL | Oral | NextWave Pharmaceuticals, Inc | NDA | View NDC → |
| 💊Extended-release tablet | ||||
| 5 mg | Oral | NextWave Pharmaceuticals, Inc | NDA | View NDC → |
| 10 mg | Oral | NextWave Pharmaceuticals, Inc | NDA | View NDC → |
| 15 mg | Oral | NextWave Pharmaceuticals, Inc | NDA | View NDC → |
| 20 mg | Oral | NextWave Pharmaceuticals, Inc | NDA | View NDC → |
| 💊Orally disintegrating tablet | ||||
| 3.1 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 6.3 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 9.4 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 12.5 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 15.7 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 18.8 mg | Oral | Neos Therapeutics, LP | NDA AUTHORIZED GENERIC | View NDC → |
| 3.1 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 6.3 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 9.4 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 12.5 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 15.7 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 18.8 mg | Oral | Neos Therapeutics Brands, LLC | NDA | View NDC → |
| 3.1 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 6.3 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 9.4 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 15.7 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 18.8 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 💊Tablet | ||||
| 5 mg | Oral | Amici Pharma, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Amici Pharma, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Amneal Pharmaceuticals NY LLC | ANDA | View NDC → |
| 10 mg | Oral | Amneal Pharmaceuticals NY LLC | ANDA | View NDC → |
| 5 mg | Oral | Aurolife Pharma, LLC | ANDA | View NDC → |
| 10 mg | Oral | Aurolife Pharma, LLC | ANDA | View NDC → |
| 5 mg | Oral | Azurity Pharmaceuticals, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Azurity Pharmaceuticals, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Bryant Ranch Prepack × 6 listings | ANDA | View NDC → |
| 10 mg | Oral | Bryant Ranch Prepack × 7 listings | ANDA | View NDC → |
| 5 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 10 mg | Oral | Dr. Reddy's Laboratories Inc | ANDA | View NDC → |
| 5 mg | Oral | Epic Pharma LLC | ANDA | View NDC → |
| 10 mg | Oral | Epic Pharma LLC | ANDA | View NDC → |
| 5 mg | Oral | Granules Pharmaceuticals Inc. | ANDA | View NDC → |
| 10 mg | Oral | Granules Pharmaceuticals Inc. | ANDA | View NDC → |
| 5 mg | Oral | Lannett Company, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Lannett Company, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Solco Healthcare US, LLC | ANDA | View NDC → |
| 10 mg | Oral | Solco Healthcare US, LLC | ANDA | View NDC → |
| 5 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 10 mg | Oral | SpecGx LLC | ANDA | View NDC → |
| 5 mg | Oral | Wilshire Pharmaceuticals, Inc. | ANDA | View NDC → |
| 10 mg | Oral | Wilshire Pharmaceuticals, Inc. | ANDA | View NDC → |
Showing 58 of 58 products — FDA National Drug Code Directory. See every product, package size and price: browse all 58 Amphetamine NDCs →
Amphetamine side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Amphetamine — 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 Amphetamine 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.
Amphetamine FDA approval history
How Amphetamine went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Amphetamine recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Amphetamine recalls since July 2021.
✅No Amphetamine recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 725 4 dose forms · 18 strengths
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Dose form (SCDF) Disintegrating Oral Tablet RxCUI 2118894In current FDA listingsClinical drug / strength (SCD) sulfate 10 MGRxCUI 2118896sulfate 15 MGRxCUI 2118898sulfate 20 MGRxCUI 2118900sulfate 5 MGRxCUI 2118895 -
Dose form (SCDF) Extended Release Oral Tablet RxCUI 1739802In current FDA listingsClinical drug / strength (SCD) 24 HR amphetamine 10 MGRxCUI 258546024 HR amphetamine 12.5 MGRxCUI 173980324 HR amphetamine 15 MGRxCUI 258546224 HR amphetamine 15.7 MGRxCUI 173981324 HR amphetamine 18.8 MGRxCUI 173981924 HR amphetamine 20 MGRxCUI 258546824 HR amphetamine 3.1 MGRxCUI 173982524 HR amphetamine 5 MGRxCUI 258547324 HR amphetamine 6.3 MGRxCUI 173983124 HR amphetamine 9.4 MGRxCUI 1739837 -
Dose form (SCDF) Extended Release Suspension RxCUI 1720585In current FDA listings -
Dose form (SCDF) Oral Tablet RxCUI 370893In current FDA listings
Look up RxCUI 725 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.
Amphetamine supply and shortage status
Whether Amphetamine is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Amphetamine costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet · Oral | 10 mg | $0.409 per tablet | NDC details & price history |
| Tablet · Oral | 5 mg | $0.425 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 12.5 mg | $15.96 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 18.8 mg | $15.61 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 15.7 mg | $15.93 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 9.4 mg | $16.22 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 6.3 mg | $16.07 per tablet | NDC details & price history |
| Tablet, Orally Disintegrating · Oral | 3.1 mg | $15.84 per tablet | NDC details & price history |
| Tablet, Extended Release · Oral | 20 mg | $14.79 per tablet | NDC details & price history |
| Tablet, Extended Release · Oral | 5 mg | $7.85 per tablet | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Amphetamine brand names
Amphetamine is sold under 8 brand names in the FDA directory — Adzenys ER, Adzenys XR, Dyanavel XR, Evekeo and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Amphetamine: manufacturers and labelers
16 companies list Amphetamine products with the FDA. By number of product records, the largest are Bryant Ranch Prepack, Neos Therapeutics Brands, LLC, Neos Therapeutics, LP. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Amphetamine drug class (RxNorm)
Amphetamine 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.
Sources for this Amphetamine page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Neos Therapeutics Brands, LLC is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →