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Two medicines, side by side

Escitalopram vs paroxetine

Escitalopram and paroxetine are both labeled for depression and anxiety. Drugs@FDA records approvals of escitalopram since 2002 and of paroxetine since 1992. Pharmacies paid $0.0632 per escitalopram 20 mg tablet and $0.0611 per paroxetine HCl 20 mg tablet (NADAC, October 7, 2026). How each works, in its label's words: Escitalopram, “The mechanism of antidepressant action of escitalopram, the S-enantiomer of racemic citalopram, is presumed to be linked to potentiation of serotonergic activity in the central nervous system (CNS) …”; Paroxetine, “The mechanism of action of paroxetine tablets in the treatment of MDD, SAD, OCD, PD, GAD, and PTSD is unknown, but is presumed to be linked to potentiation of serotonergic activity in the central …”

Check it at the source: the escitalopram FDA label on DailyMed (effective October 1, 2023); the paroxetine FDA label on DailyMed (effective February 12, 2026).

Highlights of the escitalopram record

Escitalopram (Lexapro) · label of October 1, 2023

Boxed warning

SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behaviors in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions ( 5.1 )]. Lexapro is not approved for use in pediatric patients less than 7 years of age [ s ee Use in Specific Populations ( 8.4 )].

Used for

From the label: indications

Lexapro is indicated for the treatment of: • major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. • generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older. […]

On the market

Earliest approval on file
August 14, 2002
Generic labelers
43 labelers
Pharmacy cost
$0.0632 per tablet

Supply and safety

Shortage
No current entry
Recalls
1

Highlights of the paroxetine record

Paroxetine (Paxil) · label of February 12, 2026

Boxed warning

SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behaviors in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1) ]. Paroxetine tablets are not approved for use in pediatric patients [see Use in Specific Populations (8.4) ].

Used for

From the label: indications

Paroxetine tablets are indicated in adults for the treatment of: • Major depressive disorder (MDD) • Obsessive compulsive disorder (OCD) • Panic disorder (PD) • Social anxiety disorder (SAD) • Generalized anxiety disorder (GAD) • Posttraumatic stress disorder (PTSD) Paroxetine tablets are a selective serotonin reuptake inhibitor (SSRI) indicated in adults for the treatment of ( 1 ): • Major Depressive Disorder (MDD) • Obsessive Compulsive Disorder (OCD) • Panic Disorder (PD) • Social Anxiety Disorder (SAD) • Generalized Anxiety Disorder (GAD) • Posttraumatic Stress Disorder (PTSD) […]

On the market

Earliest approval on file
December 29, 1992
Generic labelers
45 labelers
Pharmacy cost
$0.0611 per tablet

Supply and safety

Shortage
No current entry
Recalls
15

Source: FDA drug labels via openFDA (Escitalopram label of October 1, 2023, Paroxetine label of February 12, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do escitalopram and paroxetine differ on the record?

How each works, in its label's words: Escitalopram, “The mechanism of antidepressant action of escitalopram, the S-enantiomer of racemic citalopram, is presumed to be linked to potentiation of serotonergic activity in the central nervous system (CNS) …”; Paroxetine, “The mechanism of action of paroxetine tablets in the treatment of MDD, SAD, OCD, PD, GAD, and PTSD is unknown, but is presumed to be linked to potentiation of serotonergic activity in the central …”

Both are in FDA's class serotonin reuptake inhibitors.

Half-life, in each label's words: Escitalopram, “Elimination Biotransformation of escitalopram is mainly hepatic, with a mean terminal half-life of about 27-32 hours.”; Paroxetine, “Elimination Metabolism The mean elimination half-life is approximately 21 hours (CV 32%) after oral dosing of 30 mg …”

Both labels carry a boxed warning; the records quote them.

Generics: escitalopram since 2007; paroxetine since 2003 (Drugs@FDA).

EscitalopramParoxetine
Labeled forDepression, AnxietyDepression, Anxiety, Menopause symptoms
Pharmacologic classSerotonin Reuptake InhibitorSerotonin Reuptake Inhibitor
How it works (label)The mechanism of antidepressant action of escitalopram, the S-enantiomer of racemic citalopram, is presumed to be linked to potentiation of serotonergic activity in the central nervous system (CNS) resulting from its inhibition of CNS …The mechanism of action of paroxetine tablets in the treatment of MDD, SAD, OCD, PD, GAD, and PTSD is unknown, but is presumed to be linked to potentiation of serotonergic activity in the central nervous system resulting from inhibition of …
Half-life (label)Elimination Biotransformation of escitalopram is mainly hepatic, with a mean terminal half-life of about 27-32 hours.Elimination Metabolism The mean elimination half-life is approximately 21 hours (CV 32%) after oral dosing of 30 mg tablets daily for 30 days of paroxetine tablets.
Earliest approval on file (Drugs@FDA)August 14, 2002December 29, 1992
First generic approvedJuly 31, 2007July 30, 2003
Generic labelers (NDC)43 labelers45 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0632 per tablet (Escitalopram 20 mg tablet)$0.0611 per tablet (Paroxetine HCl 20 mg tablet)
12-month price change-12%-16%
Boxed warningYesYes
Shortage nowNo current entryNo current entry
Recalls recorded115
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)139,51941,809
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What do the labels say about using others of their kind?

Escitalopram label, drug interactions

Concomitant use of Lexapro and other serotonergic drugs (including other SSRIs, SNRIs, triptans, tricyclic antidepressants, opioids, lithium, buspirone, amphetamines, tryptophan, and St. John's Wort) increases the risk of serotonin syndrome.

Paroxetine label, warnings and precautions

Increased risk when co-administered with other serotonergic agents, but also when taken alone.

Source: FDA drug labels via openFDA

What next?

Alternatives to escitalopram
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