NDC 67877-0263-60
Duloxetine 20 mg/1 CAPSULE, DELAYED RELEASE
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NDC
67877-0263-60
Generic Name
Duloxetine
Brand Name
Duloxetine
Strength
20 mg/1
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Package Size
—
Labeler
Ascend Laboratories, LLC
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Duloxetine 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 neuropathic pain in adults Fibromyalgia in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults Duloxetine hydrochloride is a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of the following conditions: Major d…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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