FDA
label_change
· 2009-09-30
FDA Approved: LUNESTA — Supplemental Application (Waylis Therapeutics LLC)
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
Snippet
SUPPL AP for LUNESTA (ESZOPICLONE)