Zaleplon
| Clinical data | |||
|---|---|---|---|
| Trade names | Sonata, others | ||
| AHFS/Drugs.com | Monograph | ||
| MedlinePlus | a601251 | ||
| License data | |||
| Addiction liability | Moderate | ||
| Routes of administration | By mouth | ||
| Drug class | nonbenzodiazepine | ||
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| Pharmacokinetic data | |||
| Bioavailability | 30% (oral) | ||
| Metabolism | Liver aldehyde oxidase (91%), CYP3A4 (9%) | ||
| Metabolites | No active metabolites | ||
| Onset of action | 10 to 30 minutes | ||
| Elimination half-life | 1 hr | ||
| Duration of action | Approximately 4 to 6 hours | ||
| Excretion | Kidney | ||
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| ECHA InfoCard | 100.126.674 | ||
| Chemical and physical data | |||
| Formula | C17H15N5O | ||
| Molar mass | 305.341 g·mol−1 | ||
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Zaleplon, sold under the brand name Sonata among others, is a sedative and hypnotic which is used to treat insomnia. It is a nonbenzodiazepine or Z-drug of the pyrazolopyrimidine class. It was developed by King Pharmaceuticals and approved for medical use in the United States in 1999.