NDC 68180-0294-07
Duloxetine 20 mg/1 CAPSULE, DELAYED RELEASE
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NDC
68180-0294-07
Generic Name
Duloxetine
Brand Name
Duloxetine
Strength
20 mg/1
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Package Size
—
Labeler
Lupin Pharmaceuticals, Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Duloxetine delayed-release capsules 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 delayed-release capsules are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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