Anpheros Search · Treatment

Duloxetine

Also known as: Yentreve · Cymbalta · Duloxetine Lilly · Duloxetine Viatris (previously Duloxetine Mylan) · Duloxetine Zentiva · DULOXETINE HYDROCHLORIDE

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In short

In the European Union, duloxetine is indicated in adults for the treatment of major depressive disorder, diabetic peripheral neuropathic pain, and generalised anxiety disorder. Also in the European Union, it is indicated for women for the treatment of moderate to severe stress urinary incontinence. In the United States, duloxetine is a serotonin and norepinephrine reuptake inhibitor indicated for the treatment of major depressive disorder in adults, generalized anxiety disorder in adults and pediatric patients 7 years of age and older, and diabetic peripheral neuropathic pain in adults. Additionally, in the United States, it is indicated for the treatment of fibromyalgia in adults and pediatric patients 13 years of age and older, as well as chronic musculoskeletal pain in adults.

From: Source: European Medicines Agency (EMA), Cymbalta — EPAR, 09/07/2024. © European Medicines Agency. · Source: European Medicines Agency (EMA), Duloxetine Lilly — EPAR, 09/07/2024. © European Medicines Agency. · Source: European Medicines Agency (EMA), Yentreve — EPAR, 09/07/2024. © European Medicines Agency. · Data provided by the U.S. Food and Drug Administration.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
72625 duloxetine
EMA
EMEA/H/C/000545, EMEA/H/C/000572, EMEA/H/C/004000, EMEA/H/C/003981, EMEA/H/C/003935

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Cymbalta

Treatment of major depressive disorder. Treatment of diabetic peripheral neuropathic pain. Treatment of generalised anxiety disorder. Cymbalta is indicated in adults.

Source: European Medicines Agency (EMA), Cymbalta — EPAR, 09/07/2024. © European Medicines Agency.

Document date: 09/07/2024 · Official document →

FDA (USA) Duloxetine

1 INDICATIONS AND USAGE Duloxetine delayed-release capsule is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of the following conditions: Major depressive disorder (MDD) in adults ( 1 ) Generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older ( 1 ) Diabetic peripheral neuropathic Pain (DPNP) in adults ( 1 ) Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older ( 1 ) Chronic musculoskeletal pain in adults ( 1 ) Duloxetine delayed-release capsules are 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 neuropathic pain in adults Fibromyalgia in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults

Data provided by the U.S. Food and Drug Administration.

Document date: 20260710 · Official document →

EMA (EU) Duloxetine Lilly

Duloxetine Lilly is indicated in adults for: Treatment of major depressive disorder Treatment of diabetic peripheral neuropathic pain Treatment of generalised anxiety disorder Duloxetine Lilly is indicated in adults.

Source: European Medicines Agency (EMA), Duloxetine Lilly — EPAR, 09/07/2024. © European Medicines Agency.

Document date: 09/07/2024 · Official document →

EMA (EU) Yentreve

Yentreve is indicated for women for the treatment of moderate to severe stress urinary incontinence (SUI).

Source: European Medicines Agency (EMA), Yentreve — EPAR, 09/07/2024. © European Medicines Agency.

Document date: 09/07/2024 · Official document →

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External resources

Questions

What is Duloxetine approved for in the European Union?

Treatment of major depressive disorder. Treatment of diabetic peripheral neuropathic pain. Treatment of generalised anxiety disorder. Cymbalta is indicated in adults. (Source: European Medicines Agency (EMA), Cymbalta — EPAR, 09/07/2024. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Data provided by the U.S. Food and Drug Administration.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Cymbalta — EPAR, 09/07/2024. © European Medicines Agency.
  • Source: European Medicines Agency (EMA), Duloxetine Lilly — EPAR, 09/07/2024. © European Medicines Agency.
  • Source: European Medicines Agency (EMA), Yentreve — EPAR, 09/07/2024. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →