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These highlights do not include all the information needed to use DULOXETINE DELAYED-RELEASE CAPSULES safely and effectively. See full prescribing information for DULOXETINE DELAYED-RELEASE CAPSULES. DULOXETINE delayed-release capsules, for oral use Initial U.S. Approval: 2004
Medication labelWhy this: Advisory · dailymed-prescription
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
- generic_name
- duloxetine hydrochloride
- product_names
- Duloxetine Hydrochloride
- ndc
- 59651-279, 59651-280, 59651-282, 59651-279-60, 59651-279-99, 59651-279-10, 59651-279-78, 59651-279-71, 59651-280-30, 59651-280-90, 59651-280-99, 59651-280-10, 59651-280-78, 59651-280-59, 59651-282-30, 59651-282-90, 59651-282-99, 59651-282-10, 59651-282-78, 59651-282-39
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en