Modafinil: uses, dosing, side effects & brands
Modafinil is a sympathomimetic-like agent sold in the U.S. under one brand, for attention deficit disorder with hyperactivity, fatigue and narcolepsy. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Sympathomimetic-Like Agent
- Treats
- Attention Deficit Disorder with Hyperactivity, Fatigue and Narcolepsy
- Available as
- Tablet
- Sold as
- Modafinil
- Prescription?
- Prescription only
- Generic available?
- Yes
- What the pharmacy pays
- about $10 for a 30-count supply — not your price
How modafinil is dosed
From the FDA label for Modafinil (application ANDA207196). Other modafinil products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
The recommended dosage of modafinil tablets for each indication are as follows: Narcolepsy or OSA: 200 mg once a day in the morning. (2.1) SWD: 200 mg once a day, taken approximately one hour prior to start of the work shift (2.2) Severe Hepatic Impairment: reduce dose to half the recommended dose. (2.3, 12.3) Geriatric Patients: consider lower dose. (2.4, 12.3) 2.1 Dosage in Narcolepsy and Obstructive Sleep Apnea (OSA) The recommended dosage of modafinil tablets for patients with narcolepsy or OSA is 200 mg taken orally once a day as a single dose in the morning. Doses up to 400 mg/day, given as a single dose, have been well tolerated, but there is no consistent evidence that this dose confers additional benefit beyond that of the 200 mg/day dose [see Clinical Pharmacology (12.3) and Clinical Studies (14.1 , 14.2 )]. 2.2 Dosage in Shift Work Disorder (SWD) The recommended dosage of modafinil tablets for patients with SWD is 200 mg taken orally once a day as a single dose approximately 1 hour prior to the start of their work shift. 2.3 Dosage Modifications in Patients with Severe Hepatic Impairment In patients with severe hepatic impairment, the dosage of modafinil tablets should be reduced to one-half of that recommended for patients with normal hepatic function [see Use in Specific Populations (8.6) and Clinical Pharmacology (12.3) ]. 2.4 Use in Geriatric Patients…
Modafinil side effects
The following serious adverse reactions are described elsewhere in the labeling: Serious Rash, including Stevens-Johnson Syndrome [see Warnings and Precautions (5.1) ] Angioedema and Anaphylaxis Reactions [see Warnings and Precautions (5.2) ] Multi-organ Hypersensitivity Reactions [see Warnings and Precautions (5.3) ] Persistent Sleepiness [see Warnings and Precautions (5.4) ] Psychiatric Symptoms [see Warnings and Precautions (5.5) ] Effects on Ability to Drive and Use Machinery [see Warnings and Precautions (5.6) ] Cardiovascular Events [see Warnings and Precautions (5.7) ] Most common adverse reactions (≥5%): headache, nausea, nervousness, rhinitis, diarrhea, back pain, anxiety, insomnia, dizziness, and dyspepsia. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Avet Pharmaceuticals Inc. at 1-866-901-3784 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Modafinil tablets has been evaluated for safety in over 3,500 patients, of whom more than 2,000 patients with excessive sleepiness associated with OSA, SWD, and narcolepsy. Most Common Adverse Reactions In placebo-controlled…
Who shouldn’t take modafinil
Modafinil tablets are contraindicated in patients with known hypersensitivity to modafinil or armodafinil or its inactive ingredients [see Warnings and Precautions (5.1, 5.2 , 5.3) ]. Modafinil tablets are contraindicated in patients with known hypersensitivity to modafinil or armodafinil.
Modafinil drug interactions
Effects of Modafinil Tablets on CYP3A4/5 Substrates The clearance of drugs that are substrates for CYP3A4/5 (e.g., steroidal contraceptives, cyclosporine, midazolam, and triazolam) may be increased by modafinil tablets via induction of metabolic enzymes, which results in lower systemic exposure. Dosage adjustment of these drugs should be considered when these drugs are used concomitantly with modafinil tablets [see Clinical Pharmacology (12.3) ]. The effectiveness of steroidal contraceptives may be reduced when used with modafinil tablets and for one month after discontinuation of therapy. Alternative or concomitant methods of contraception are recommended for patients taking steroidal contraceptives (e.g., ethinyl estradiol) when treated concomitantly with modafinil tablets and for one month after discontinuation of modafinil tablets treatment. Blood levels of cyclosporine may be reduced when used with modafinil tablets. Monitoring of circulating cyclosporine concentrations and appropriate dosage adjustment for cyclosporine should be considered when used concomitantly with modafinil tablets. Effects of Modafinil Tablets on CYP2C19 Substrates Elimination of drugs that are substrates for CYP2C19 (e.g., phenytoin, diazepam, propranolol, omeprazole, and clomipramine) may be prolonged by modafinil tablets via inhibition of metabolic enzymes, with resultant higher systemic exposure. In individuals deficient in the CYP2D6 enzyme, the levels of CYP2D6 substrates which have ancillary routes of elimination through CYP2C19, such as tricyclic antidepressants and selective serotonin reuptake inhibitors, may be increased by co-administration of modafinil tablets. Dose adjustments of these drugs and other drugs that are substrates for CYP2C19 may be necessary when used concomitantly with modafinil tablets [see Clinical Pharmacology (12.3) ]. Warfarin More frequent monitoring of prothrombin times/INR should be considered whenever modafinil tablets are coadministered with warfarin [see Clinical Pharmacology (12.3) ]. Monoamine Oxidase (MAO) Inhibitors Caution should be used when concomitantly administering MAO inhibitors and modafinil tablets. Steroidal contraceptives (e.g., ethinyl estradiol): Use alternative or concomitant methods of contraception while taking modafinil tablets and for one month after discontinuation of modafinil tablets treatment. (7) Cyclosporine: Blood concentrations of cyclosporine may be reduced. (7) CYP2C19 substrates, such as omeprazole, phenytoin, and diazepam: Exposure of these medications may be increased. (7)
Every modafinil product we track (1)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
Only one: Modafinil.
What modafinil pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
Modafinil and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for modafinil: levels in milk, effects in breastfed infants, and the drugs it would consider insteadLittle information is available on the excretion of modafinil into breastmilk. In the case reports available, only R-modafinil was measured. R-enantiomer is the predominant form (about 75%) in the blood after administration of racemic modafinil, but not measuring S-modafinil in those reports likely led to an underreporting of the total amount in milk and exposure in the infant. Nevertheless, milk levels of R-modafinil in two nursing mothers and serum of one breastfed infant were very low. Some information from women who breastfed their infants while using modafinil found no adverse effects in the infants. Until more safety data are available, modafinil should be used with careful infant monitoring during breastfeeding, or an alternate drug may be preferred.
National Institute of Child Health and Human Development, record revised April 15, 2025. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about modafinil
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 16,693 reports naming modafinil, and the FDA flagged 62% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- fatigue1,544 reports
- nausea1,204 reports
- headache1,011 reports
- fall958 reports
- depression864 reports
- anxiety841 reports
- somnolence787 reports
- dizziness780 reports
Read these as a signal, not a rate. A report does not mean modafinil caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.
Source: openFDA drug/event (FAERS), retrieved July 25, 2026.
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Frequently asked questions
What is modafinil?
Modafinil is a sympathomimetic-like agent used to treat Attention Deficit Disorder with Hyperactivity, Fatigue, Narcolepsy, Obstructive Sleep Apnea.
What kind of drug is modafinil?
The FDA classifies modafinil as a sympathomimetic-like agent. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.
Can you take modafinil with other medicines?
It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run modafinil against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What forms does modafinil come in?
Across the brands we track, modafinil is currently marketed as tablet, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.
Is there a generic modafinil?
Yes. Our catalog lists 1 generic modafinil product alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.
Cite this page
- APA
- pharmaranks. (2026, July 24). Modafinil: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/modafinil
- MLA
- “Modafinil: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/modafinil.
We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Read the full FDA label for modafinil on DailyMed (NIH) ↗.