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AboutPricing
Drug ReportsEscitalopram
Escitalopram
Escitalopram Oxalate, Lexapro (escitalopram) is a small molecule pharmaceutical. Escitalopram was first approved as Lexapro on 2002-08-14. It is used to treat major depressive disorder in the USA. The pharmaceutical is active against sodium-dependent serotonin transporter.
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Events Timeline
5D
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3M
6M
YTD
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FDA approval date
EMA approval date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
mental disordersD001523
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
Brand Name
Status
Last Update
escitalopramANDA2024-11-11
escitalopram oral solutionANDA2023-09-01
escitalopram oxalateANDA2024-11-07
lexaproNew Drug Application2023-11-17
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
Expiration
Code
ESCITALOPRAM OXALATE, LEXAPRO, ABBVIE
2026-05-12NPP
Patent Expiration
No data
ATC Codes
N: Nervous system drugs
N06: Psychoanaleptics
N06A: Antidepressants
N06AB: Selective serotonin reuptake inhibitors
N06AB10: Escitalopram
HCPCS
No data
Clinical
Clinical Trials
692 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
DepressionD003863F33.9225877129105375
Depressive disorderD003866EFO_1002014F32.A25628012996374
Major depressive disorderD003865EFO_0003761F221545538059244
Anxiety disordersD001008EFO_0006788F41.15612151449
Healthy volunteers/patients244735
AnxietyD001007EFO_0005230F41.1156718
SyndromeD0135772436618
Obsessive-compulsive disorderD009771EFO_0004242F42129517
Compulsive personality disorderD003193F60.5128516
Bipolar disorderD001714EFO_0000289F30.91244515
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Indications Phases 2
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Drug-related side effects and adverse reactionsD064420T88.755
Taste disordersD01365133
CognitionD003071EFO_000392533
PharmacokineticsD01059922
DiseaseD004194EFO_0000408R6922
Adolescent developmentD04192322
Affective symptomsD00034222
PerimenopauseD04764811
Chronic painD059350HP_001253211
Intractable painD01014811
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameEscitalopram
INNescitalopram
Description
Escitalopram is a 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-5-carbonitrile that has S-configuration at the chiral centre. It is the active enantiomer of citalopram. It has a role as an antidepressant and an EC 3.4.21.26 (prolyl oligopeptidase) inhibitor. It is a conjugate base of an escitalopram(1+). It is an enantiomer of a (R)-citalopram.
Classification
Small molecule
Drug classSelective serotonin reuptake inhibitor (SSRI)
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
CN(C)CCC[C@@]1(c2ccc(F)cc2)OCc2cc(C#N)ccc21
Identifiers
PDB
CAS-ID128196-01-0
RxCUI
ChEMBL IDCHEMBL1508
ChEBI ID36791
PubChem CID146570
DrugBankDB01175
UNII ID4O4S742ANY (ChemIDplus, GSRS)
Target
Agency Approved
SLC6A4
SLC6A4
Organism
Homo sapiens
Gene name
SLC6A4
Gene synonyms
HTT, SERT
NCBI Gene ID
Protein name
sodium-dependent serotonin transporter
Protein synonyms
5-hydroxytryptamine (serotonin) transporter, 5HT transporter, 5HTT, Na+/Cl- dependent serotonin transporter, serotonin transporter 1, solute carrier family 6 (neurotransmitter transporter), member 4, solute carrier family 6 (neurotransmitter transporter, serotonin), member 4, Solute carrier family 6 member 4
Uniprot ID
Mouse ortholog
Slc6a4 (15567)
sodium-dependent serotonin transporter (Q60857)
Alternate
No data
Variants
No data
Financial
Revenue by drug
$
£
No data
Estimated US medical usage
Escitalopram
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 16,182 documents
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Safety
Black-box Warning
Black-box warning for: Escitalopram, Escitalopram oral solution, Escitalopram oxalate, Lexapro
Adverse Events
Top Adverse Reactions
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34,994 adverse events reported
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