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|Trade names||Provigil, Alertec, Modavigil, others|
|License data||US FDA: Modafinil|
|Pregnancy category||AU: B3 US: C (Risk not ruled out) |
|Dependence liability||Psychological: Very low  Physical: Negligible |
|Addiction liability||Very low to low |
|Routes of administration||By mouth (tablets) |
|ATC code||N06BA07 ( WHO )|
|Legal status||AU: S4 (Prescription only) UK: POM (Prescription only) US: Schedule IV|
|Bioavailability||Not determined due to the aqueous insolubility|
|Metabolism||Hepatic (primarily via amide hydrolysis;  CYP1A2, CYP2B6, CYP2C9, CYP2C19, CYP3A4, CYP3A5 involved |
|Elimination half-life||15 hours ( R -enantiomer), 4 hours ( S -enantiomer) |
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For entry into these studies, all patients were required to have objectively documented excessive daytime sleepiness, via a Multiple Sleep Latency Test MSLT with two or more sleep onset REM periods and the absence of any other clinically significant active medical or psychiatric disorder.Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug Read the entire FDA prescribing information for Provigil Modafinil ead the Provigil User Reviews Provigil Patient Information is supplied by Cerner Multum, Inc.
and Provigil Consumer information is supplied by First Databank, Inc. used under license and subject to their respective copyrights. hat is Provigil and how is it used?
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