(R)-(−)-citalopram (top),
(S)-(+)-citalopram (bottom) |
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Clinical data | |
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Pronunciation | /saɪˈtæləˌpræm, sɪ-/; |
Trade names | Celexa, Cipramil, others (see below) |
AHFS/Drugs.com | Monograph |
MedlinePlus | a699001 |
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Routes of administration |
Oral |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | 80% peak at 4 h |
Metabolism | Liver (CYP3A4 and CYP2C19) |
Metabolites | Desmethylcitalopram (DCT) and didesmethylcitalopram (DDCT) |
Biological half-life | 35 h |
Excretion | Mostly as unmetabolized citalopram, partly DCT and traces of DDCT in urine |
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CAS Number | |
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ChEMBL | |
ECHA InfoCard | 100.056.247 |
Chemical and physical data | |
Formula | C20H21FN2O |
Molar mass | 324.392 g/mol |
3D model (Jmol) | |
Chirality | Racemic mixture |
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Citalopram (brand names: Celexa, Cipramil and others) is an antidepressant drug of the selective serotonin reuptake inhibitor (SSRI) class. It has U.S. Food and Drug Administration approval to treat major depression, which it received in 1998, and is prescribed off-label for other conditions. In Australia, the UK, Germany, Portugal, Poland, and most European countries, it is licensed for depressive episodes and panic disorder with or without agoraphobia. In Spain and Denmark it is also used for obsessive-compulsive disorder.
In the National Institute for Health and Clinical Excellence ranking of 10 antidepressants for efficacy and cost-effectiveness citalopram is fifth in effectiveness (after mirtazapine, escitalopram, venlafaxine, and sertraline) and fourth in cost-effectiveness. The ranking results were based on the meta-analysis by Andrea Cipriani. In another analysis by Cipriani, citalopram was found to be more efficacious than paroxetine and reboxetine, and more acceptable than tricyclics, reboxetine, and venlafaxine, but less efficacious than escitalopram.
Evidence for effectiveness of citalopram for treating depression in children is uncertain.