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FDA label_change · 2009-09-30

FDA Approved: LUNESTA — Supplemental Application (Waylis Therapeutics LLC)

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Summary

FDA approved a supplemental application for Lunesta (eszopiclone) from Waylis Therapeutics LLC, resulting in a label change for the product.

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Diseases / indications

Drugs mentioned

  • Lunesta (eszopiclone)

Snippet

SUPPL AP for LUNESTA (ESZOPICLONE)