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duloxetine 20 MG Delayed Release Oral Capsule

1 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 Chronic musculoskeletal pain in adults Additional pediatric use information is approved for Eli Lilly and Company, Inc.'s CYMBALTA (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company Inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 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 ( 1 ) Chronic musculoskeletal pain in adults ( 1 )

Golden State Medical Supply


4 weeks ago CAPSULE YELLOW B 746 duloxetine 20 MG Delayed Release Oral Capsule

CAPSULE YELLOW B 746

4 weeks ago CAPSULE YELLOW B 746 duloxetine 20 MG Delayed Release Oral Capsule

B 746 CAPSULE YELLOW

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 60 mg 1 Body color Opaque ochre Opaque white Opaque ochre Cap color Opaque ochre Opaque green Opaque green Cap imprint B B B Body imprint 746 747 748 Presentations and NDC Codes Bottles of 30 NA 60429-165-30 60429-166-30 Bottles of 60 60429-164-60 NA NA Bottles of 90 NA 60429-165-90 NA Bottles of 500 NA NA NA Bottles of 1000 NA NA 60429-166-10 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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