Ingredient

Duloxetine Hydrochloride Enteric-Coated Granules

Duloxetine hydrochloride delayed-release granules are a central nervous system medication used to treat depression and anxiety disorders.

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MFDS ingredient code M259598

What does it do?

Duloxetine hydrochloride delayed-release granules are an antidepressant that inhibits the reuptake of serotonin and norepinephrine. They are primarily used to treat depression and anxiety disorders, playing a role in regulating the balance of neurotransmitters in the nervous system.

This ingredient blocks the reuptake of serotonin and norepinephrine, which regulate mood and emotions in the brain, thereby increasing the concentration of these neurotransmitters. As a result, feelings of depression improve and anxiety symptoms are alleviated.

Commonly used for

Approved uses differ by product. Check each product's information for its actual use.

Good to know

Duloxetine hydrochloride is characterized by its ability to act simultaneously on both serotonin and norepinephrine neurotransmitters. This distinguishes it from other antidepressants that act only on a single neurotransmitter.

Medicines containing this ingredient

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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Even with the same ingredient, dosage and approved uses can differ by strength, dosage form and combined ingredients. Check each product's information before taking it.

Questions about this ingredient

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For anything that needs medical judgment, consult a doctor or pharmacist.

SourceKorea Ministry of Food and Drug Safety (Drug Safety Korea)

Product approval information is based on drug information provided by the Ministry of Food and Drug Safety.
Ingredient and class descriptions are not part of MFDS data and were written separately by Cashdoc.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.