duloxetine 40 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 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 )

bluepoint laboratories

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] fatigue` `[3] nausea` `[4] toxicity to various agents` `[5] off label use` `[6] pain` `[7] headache` `[8] completed suicide` `[9] diarrhoea` `[10] dizziness`

4 years ago

CAPSULE ORANGE B 750

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 40 mg Body color Opaque orange Cap color Opaque blue Cap imprint B Body imprint 750 Presentations and NDC Codes Bottles of 30 68001-368-04 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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duloxetine 40 MG Delayed Release Oral Capsule

FDA Reported Adverse Reactions [1] drug ineffective [2] fatigue [3] nausea [4] toxicity to various agents [5] off label use [6] pain [7] headache [8] completed suicide [9] diarrhoea [10] dizziness

CAPSULE ORANGE B 750

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FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] fatigue` `[3] nausea` `[4] toxicity to various agents` `[5] off label use` `[6] pain` `[7] headache` `[8] completed suicide` `[9] diarrhoea` `[10] dizziness`