COMPOUNDS / NOOTROPIC / ARMODAFINIL
NOOTROPIC

ARMODAFINIL

LOW RISK
BEST FOR:Wakefulness●●●●●●●●●○9/10
ARMODAFINIL · NUVIGIL · R-MODAFINIL · (R)-(-)-MODAFINIL · CRL-40982
Wakefulness AgentNootropicEugeroicPrescriptionStimulant

The R-enantiomer of modafinil; a long-acting wakefulness-promoting agent prescribed for narcolepsy, sleep apnea, and shift work disorder.

ROUTE / DOSAGE
LOW50mg
STANDARD150-250mg
HIGH300mg+
Note: Take in morning; late dosing risks insomnia due to long half-life
CYCLE
Daily use acceptable for prescribed indications for off-label cognitive use limit to 2-3x per week
BIOAVAILABILITY
~80% oral
ACTIVE DURATION
8-15h (subjective)
STORAGE
Room temperature dry away from light
HALF-LIFE
10-15h (plasma)
DURATION BREAKDOWN
Total8-15 hours
Onset20-60 min
Come up1-2.5 hours
Peak2-6 hours
Offset4-8 hours
After effects4-12 hours
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
6 documented
Promoted wakefulness and alertness
Reduced excessive daytime sleepiness
Improved sustained attention
Enhanced working memory
Decreased perception of fatigue
Prolonged focus and concentration
§ 02 — RISKS
Insomnia and sleep disturbance (significantly increased risk vs placebo)
Headache (common, especially initially)
Nausea and gastrointestinal discomfort
Increased adverse events leading to treatment withdrawal
Potential reduced efficacy of hormonal contraceptives
Rare serious skin reactions including Stevens-Johnson syndrome (class effect)
§ 03 — INTERACTIONS
No interaction with your stack
VIEW STACK
CAUTION
Alcohol
MXE
Dissociatives
AVOID · DANGEROUS
25x-NBOMe
25x-NBOH
Tramadol
MAOIs
Hormonal birth control
DXM
MDMA
Stimulants
§ 04 — SCIENCE

Four large double-blind multinational trials (n > 195 each, 12 weeks) demonstrated that once-daily armodafinil (150 or 250 mg) significantly improved wakefulness in narcolepsy, obstructive sleep apnea, and shift work sleep disorder compared to placebo. A meta-analysis in res-OSA found improvements in subjective and objective sleepiness but noted tripled adverse events and doubled withdrawals due to adverse events. A systematic review and meta-analysis in post-TBI excessive daytime sleepiness showed modest ESS improvement but significantly increased insomnia risk. Evidence for ADHD treatment in adults is scarce but suggests potential benefit in wakefulness, memory, and executive function. Armodafinil is classified as Schedule IV with low abuse potential.

§ 06 — SOURCES
[1]
Armodafinil - CNS Drugs 2009
pubmed.ncbi.nlm.nih.gov ↗
[2]
Armodafinil as Potential Treatment for ADHD in Adults - Curr Neuropharmacol 2024
pubmed.ncbi.nlm.nih.gov ↗
[3]
Armodafinil in Milk - J Hum Lact 2023
pubmed.ncbi.nlm.nih.gov ↗
[4]
Modafinil/armodafinil for EDS after TBI: Meta-analysis - Brain Inj 2025
pubmed.ncbi.nlm.nih.gov ↗
[5]
Armodafinil in the treatment of excessive sleepiness - Expert Opin Pharmacother 2010
pubmed.ncbi.nlm.nih.gov ↗
[6]
Modafinil/armodafinil in OSA: Meta-analysis - Eur Respir J 2016
pubmed.ncbi.nlm.nih.gov ↗
[7]
Headache improves with armodafinil - J Clin Sleep Med 2024
pubmed.ncbi.nlm.nih.gov ↗
[8]
Armodafinil for excessive daytime sleepiness - Drugs Today 2008
pubmed.ncbi.nlm.nih.gov ↗
[9]
PsychonautWiki - Armodafinil
psychonautwiki.org ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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