Duloxetine D/R

FDA Drug Profile — Duloxetine D/R

Drug Details

Generic Name
Duloxetine D/R
Brand Names
Duloxetine D/R
Application Number
ANDA208706
Sponsor
Direct_Rx
NDC Codes
4
Dosage Forms
CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients
DULOXETINE HYDROCHLORIDE

Indications and Usage

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