DULOXETINE duloxetine 60 MG Delayed Release Oral Capsule
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 of the following conditions: Major Depressive disorder (MDD) in adults ( 1 ) Generalized Anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older ( 1 ) Diabetic peripheral neuropathic pain (DPNP) in adults ( 1 ) Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older ( 1 ) Chronic Musculoskeletal Pain in adults ( 1 )
Breckenridge Pharmaceutical, Inc.
CAPSULE GREEN B 748
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16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied Duloxetine delayed-release capsules, USP are available in the following strengths, colors, imprints, and presentations: Features Strengths 20 mg equivalent to duloxetine base 30 mg 40 mg 60 mg Body color Opaque ochre Opaque white Opaque orange Opaque ochre Cap color Opaque ochre Opaque green Opaque blue Opaque green Cap imprint B B B B Body imprint 746 747 750 748 Presentations and NDC Codes Bottles of 30 NA 51991-747-33 51991-750-33 51991-748-33 Bottles of 60 51991-746-06 NA NA NA Bottles of 90 51991-746-90 51991-747-90 51991-750-90 51991-748-90 Bottles of 500 51991-746-05 NA 51991-750-05 NA Bottles of 1000 NA 51991-747-10 51991-750-10 51991-748-10 16.2 Storage and Handling Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature].
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