FDA Approved: CYMBALTA — Supplemental Application (Eli Lilly and Company)

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Summary

The FDA approved a supplemental application for Cymbalta (duloxetine hydrochloride) submitted by Eli Lilly and Company.

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Diseases / indications

• Diabetic Peripheral Neuropathy
• Fibromyalgia
• Generalized Anxiety Disorder
• Low Back Pain
• Major Depressive Disorder
• Musculoskeletal Pain
• Osteoarthritis

Drugs mentioned

• Cymbalta (duloxetine)

Snippet

SUPPL AP for CYMBALTA (DULOXETINE HYDROCHLORIDE)