Comprehensive medication guide to Levetiracetam including estimated pricing, availability information, side effects, and how to find it in stock at your local pharmacy.
Estimated Insurance Pricing
$0–$30 copay for generic on most commercial plans and Medicare Part D (Tier 1–2); prior authorization uncommon for generic. Brand Keppra may require step therapy or prior authorization.
Estimated Cash Pricing
$65–$153 retail for generic levetiracetam 500 mg (30-day supply); as low as $6–$7 with GoodRx or SingleCare coupons. Extended-release generic is approximately $114 retail or $15–$16 with coupons.
Medfinder Findability Score
72/100
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Levetiracetam is a prescription antiepileptic drug (AED) used to treat epilepsy in adults and children. Sold under brand names including Keppra, Keppra XR, Spritam, and Roweepra, it is one of the most commonly prescribed seizure medications in the United States—with more than 6 million prescriptions dispensed annually. Generic levetiracetam has been available since 2008, making it substantially more affordable than the original brand.
The FDA first approved levetiracetam in 1999 for partial-onset (focal) seizures, and expanded its indications to include myoclonic seizures in juvenile myoclonic epilepsy (2005) and primary generalized tonic-clonic seizures (2006). Intravenous levetiracetam was approved in 2006 for hospital use. Levetiracetam is approved for patients as young as 1 month of age for partial-onset seizures.
Levetiracetam is available in multiple formulations: immediate-release tablets (250 mg, 500 mg, 750 mg, 1000 mg), extended-release tablets (500 mg, 750 mg), oral solution (100 mg/mL), orally disintegrating tablets (Spritam), and intravenous solution for hospital use. It is not a controlled substance under U.S. federal law.
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Levetiracetam works through a novel mechanism that is fundamentally different from all older antiepileptic drugs. Its primary target is the synaptic vesicle glycoprotein SV2A—a protein found on the surface of synaptic vesicles (the tiny packets that store neurotransmitters inside nerve cells). By binding to SV2A, levetiracetam modulates how vesicles release neurotransmitters during high-frequency neuronal firing, selectively dampening the abnormal, synchronized bursts of activity that characterize seizures.
Unlike older AEDs such as phenytoin, carbamazepine, or valproic acid, levetiracetam does NOT inhibit voltage-gated sodium channels, does NOT affect GABA receptors, and does NOT bind to glutamate receptors. This unique, non-overlapping mechanism explains why it is effective for patients who don't respond to other AEDs and why it has so few drug interactions. Levetiracetam also inhibits presynaptic calcium channels, providing an additional brake on excessive neurotransmitter release.
Pharmacokinetically, levetiracetam is nearly ideal: it has close to 100% oral bioavailability, is minimally protein-bound (<10%), is not significantly metabolized by the liver (66% excreted unchanged by the kidneys), and has few drug-drug interactions. Plasma half-life is 6–8 hours; steady-state is reached in just 2 days. Dose adjustment is required for renal impairment.
250 mg — tablet (immediate-release)
Starting/low dose; useful for pediatric and renal-adjusted dosing
500 mg — tablet (immediate-release)
Most common adult starting dose (500 mg twice daily)
750 mg — tablet (immediate-release)
Intermediate dose for titration
1000 mg — tablet (immediate-release)
Higher dose tablet for simplified dosing
500 mg — tablet (extended-release)
Once-daily formulation; Keppra XR / Elepsia XR
750 mg — tablet (extended-release)
Once-daily extended-release formulation
100 mg/mL — oral solution
Grape-flavored liquid; for children and patients who cannot swallow tablets
250–1000 mg — orally disintegrating tablet (Spritam)
3D-printed tablet that dissolves in water on the tongue
100 mg/mL — IV solution
For hospital/inpatient use when oral administration not possible
As of 2026, there is no active national FDA shortage of oral levetiracetam immediate-release tablets in the United States. Generic levetiracetam is produced by multiple manufacturers including Apotex, Lupin, Torrent, Sun Pharma, and Teva, providing redundancy in the supply chain. The findability score of 72/100 reflects that while the medication is generally available, localized spot shortages at individual pharmacy locations remain common.
Levetiracetam has a history of supply disruptions: the most significant national shortage occurred in 2019–2020, when the FDA listed multiple generic manufacturers as having supply issues. The injectable formulation experienced documented supply issues in 2024. UK patients faced branded tablet shortages into early 2025. A 2024 survey found 62.8% of epilepsy patients had experienced difficulty finding levetiracetam—a figure that substantially exceeds what national shortage data would suggest, reflecting the impact of local spot shortages.
If your pharmacy is out of levetiracetam, medfinder can call pharmacies near you to find which ones have your specific medication in stock—saving you hours of phone calls and preventing dangerous medication gaps.
Levetiracetam is not a controlled substance, so there are no DEA-based prescribing restrictions. Any licensed prescriber can write a prescription, and it can be filled at any licensed pharmacy without schedule-related limitations. For new epilepsy diagnoses, a neurologist is strongly recommended; for established patients with well-controlled seizures, primary care providers commonly manage ongoing refills.
Telehealth is available for established patients needing follow-up visits and prescription refills. Since levetiracetam is not a controlled substance, telehealth prescribing does not require in-person visits under current federal regulations. A new seizure diagnosis, however, typically requires in-person evaluation including EEG and MRI before initiating treatment.
No. Levetiracetam is not a controlled substance under U.S. federal law. It has no DEA scheduling (Schedule I through V). It does not have recognized abuse potential, does not cause physical dependence in the way controlled substances do, and is not associated with euphoria or misuse.
This means there are no federal restrictions on the number of refills, no requirement for paper prescriptions, no limits on early refills based on DEA rules, and no restrictions on transferring the prescription between pharmacies. Any licensed prescriber can prescribe levetiracetam without DEA authorization. Patients can fill it at any licensed pharmacy. This non-controlled status is a practical advantage when dealing with local stock-outs—patients can simply move their prescription to a pharmacy that has it.
Common side effects (occurring in more than 5% of patients in clinical trials):
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Lamotrigine (Lamictal)
Broad-spectrum AED; favorable side effect profile; fewer behavioral side effects than levetiracetam; requires slow titration due to SJS risk
Brivaracetam (Briviact)
Same SV2A mechanism as levetiracetam but higher binding affinity; fewer behavioral side effects; more expensive, fewer generic options
Valproic acid / divalproex (Depakote)
Broad-spectrum; effective for multiple seizure types; contraindicated in pregnancy and women of childbearing age without adequate contraception
Topiramate (Topamax)
Broad-spectrum; also used for migraine prevention; associated with cognitive side effects and weight loss
Oxcarbazepine (Trileptal)
Sodium channel blocker effective for focal seizures; fewer interactions than carbamazepine; not effective for generalized seizures
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Opioids (codeine, oxycodone, oxymorphone)
majorAdditive CNS depression; increased risk of sedation and respiratory depression. Avoid or use alternative.
Alcohol
majorAdditive CNS depression; also lowers seizure threshold. Avoid or strictly limit use.
Enzyme-inducing AEDs (carbamazepine, phenytoin, phenobarbital)
moderateIncrease levetiracetam clearance by 9–22%, potentially reducing efficacy. Dose adjustment may be needed.
Valproic acid (Depakote)
moderateDecreases levetiracetam clearance by ~18.8%; may increase levetiracetam levels and side effects.
Orlistat (Alli, Xenical)
moderateReduces oral absorption of levetiracetam, potentially causing breakthrough seizures. Monitor closely.
CNS depressants (benzodiazepines, muscle relaxants, antihistamines)
moderateAdditive sedation and CNS depression. Use with caution; monitor for excessive drowsiness.
Dabigatran / rivaroxaban
moderateLevetiracetam may decrease levels of these anticoagulants by an unknown mechanism. Monitor anticoagulation.
Cannabis (THC/CBD)
moderateCNS depression additive; unpredictable interactions with seizure threshold. Disclose to neurologist.
Levetiracetam remains one of the most important antiepileptic drugs in modern epilepsy treatment. Its novel mechanism of action (SV2A binding), favorable pharmacokinetic profile, low drug interaction burden, non-controlled status, and wide age range of approval make it a versatile first- and second-line option for most seizure types. Generic availability since 2008 has made it accessible to patients at price points as low as $6 per month with discount coupons.
The main challenges with levetiracetam are behavioral side effects (irritability, aggression—the so-called "Keppra rage") in 5–15% of patients, and the risk of rare but serious reactions including DRESS and Stevens-Johnson syndrome. Patients and caregivers should be counseled on these risks at initiation. Never stop levetiracetam abruptly—always taper under physician guidance.
If you're having trouble finding levetiracetam at your local pharmacy, medfinder can help. medfinder calls pharmacies near you to find which ones have your medication in stock—so you can focus on managing your health, not hunting for your prescription.
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