Lormetazepam
| Clinical data | |
|---|---|
| Trade names | Noctamid, Loramet, others |
| Other names | Methyllorazepam; Methyl-lorazepam; N-Methyllorazepam; Ro 5-5516 |
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| Routes of administration | Oral, intravenous |
| Drug class | Benzodiazepine |
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| Pharmacokinetic data | |
| Bioavailability | 80% |
| Metabolism | Hepatic |
| Elimination half-life | 10–12 hours |
| Excretion | Renal |
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| ECHA InfoCard | 100.011.546 |
| Chemical and physical data | |
| Formula | C16H12Cl2N2O2 |
| Molar mass | 335.18 g·mol−1 |
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Lormetazepam, sold under the brand name Noctamid among others, is a drug which is a short to intermediate acting 3-hydroxy benzodiazepine derivative and temazepam analogue. It possesses hypnotic, anxiolytic, anticonvulsant, sedative, and skeletal muscle relaxant properties.
It was patented in 1961 and came into medical use in 1980. Lormetazepam is not approved for sale in the United States or Canada. It is licensed in the UK as 0.5 and 1 mg tablets for short-term treatment (2–4 weeks) of moderately severe insomnia. It is licensed in the Netherlands as 1 and 2 mg tablets, under the brand names Loramet and Noctamid and as generic, available from several manufacturers. It is sold in Poland as Noctofer. It is also sold in France as generic as 1 and 2mg tablets, with a maximum prescription duration of 4 weeks. A Dutch analysis stated that lormetazepam could be suitable to be included in drug prescribing formularies, although zolpidem, zopiclone, and temazepam appear better.