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Two medicines, side by side

Mirtazapine vs duloxetine

Mirtazapine and duloxetine are both labeled for depression. Drugs@FDA records approvals of mirtazapine since 1996 and of duloxetine since 2004. Pharmacies paid $0.063 per mirtazapine 15 mg tablet and $0.102 per duloxetine HCl DR 30 mg capsule (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like.

Check it at the source: the mirtazapine FDA label on DailyMed (effective August 6, 2025); the duloxetine FDA label on DailyMed (effective May 14, 2024).

Highlights of the mirtazapine record

Mirtazapine (Remeron) · label of August 6, 2025

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) ]. REMERON/REMERONSolTab is not approved for use in pediatric patients [see Use in Specific Populations (8.4) ].

Used for

From the label: indications

REMERON/REMERONSolTab are indicated for the treatment of major depressive disorder (MDD) in adults [see Clinical Studies (14) ]. REMERON/REMERONSolTab is indicated for the treatment of major depressive disorder (MDD) in adults.

On the market

Earliest approval on file
June 14, 1996
Generic labelers
36 labelers
Pharmacy cost
$0.063 per tablet

Supply and safety

Shortage
No current entry
Recalls
5

Highlights of the duloxetine record

Duloxetine (Cymbalta) · label of May 14, 2024

Boxed warning

SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior 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)]. WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning.

Used for

From the label: indications

DRIZALMA SPRINKLE is indicated for the treatment of: • Major Depressive Disorder in adults • Generalized Anxiety Disorder in adults and pediatric patients 7 years of age and older • Diabetic Peripheral Neuropathy in adults • Fibromyalgia in adults • Chronic Musculoskeletal Pain in adults Additional pediatric use information is approved for Eli Lilly and Company, Inc.’s CYMBALTA (duloxetine delayed-release capsules). […]

On the market

Earliest approval on file
August 3, 2004
Generic labelers
45 labelers
Pharmacy cost
$0.102 per capsule

Supply and safety

Shortage
No current entry
Recalls
56

Source: FDA drug labels via openFDA (Mirtazapine label of August 6, 2025, Duloxetine label of May 14, 2024); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do mirtazapine and duloxetine differ on the record?

How each works, in its label's words: Mirtazapine, “The mechanism of action of mirtazapine for the treatment of major depressive disorder, is unclear.”; Duloxetine, “Although the exact mechanisms of the antidepressant, central pain inhibitory and anxiolytic actions of duloxetine in humans are unknown, these actions are believed to be related to its potentiation …”

Half-life, in each label's words: Mirtazapine, “Elimination Mirtazapine has a half-life of about 20 to 40 hours following oral administration of REMERON or …”; Duloxetine, “Mean terminal half-life was 12.4 hours (range 7.8 to 22.2 hour) in subjects receiving a single dose DRIZALMA SPRINKLE.”

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

Generics: mirtazapine since 2003; duloxetine since 2013 (Drugs@FDA).

MirtazapineDuloxetine
Labeled forDepressionDepression, Anxiety, Nerve pain and fibromyalgia, Pain
Pharmacologic classn/aSerotonin and Norepinephrine Reuptake Inhibitor
How it works (label)The mechanism of action of mirtazapine for the treatment of major depressive disorder, is unclear.Although the exact mechanisms of the antidepressant, central pain inhibitory and anxiolytic actions of duloxetine in humans are unknown, these actions are believed to be related to its potentiation of serotonergic and noradrenergic …
Half-life (label)Elimination Mirtazapine has a half-life of about 20 to 40 hours following oral administration of REMERON or REMERONSolTab.Mean terminal half-life was 12.4 hours (range 7.8 to 22.2 hour) in subjects receiving a single dose DRIZALMA SPRINKLE.
Earliest approval on file (Drugs@FDA)June 14, 1996August 3, 2004
First generic approvedJanuary 24, 2003December 11, 2013
Generic labelers (NDC)36 labelers45 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.063 per tablet (Mirtazapine 15 mg tablet)$0.102 per capsule (Duloxetine HCl DR 30 mg capsule)
12-month price change-12%+31%
Boxed warningYesYes
Shortage nowNo current entryNo current entry
Recalls recorded556
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)91,05769,298
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?

Mirtazapine label, warnings and precautions

Increased risk when co-administered with other serotonergic drugs (e.g., SSRI, SNRI, triptans), but also when taken alone.

Duloxetine label, drug interactions

Examples Selegiline, tranylcypromine, isocarboxazid, phenelzine, linezolid, intravenous methylene blue Other Serotonergic Drugs Clinical Impact Concomitant use of duloxetine with other serotonergic drugs increases the risk of serotonin syndrome.

Source: FDA drug labels via openFDA

What next?

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