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FDA approval · 2008-03-20

FDA Approved: SEREVENT DISKUS — Supplemental Application (GlaxoSmithKline LLC)

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Summary

The FDA approved a supplemental application for SEREVENT DISKUS (salmeterol xinafoate) submitted by GlaxoSmithKline LLC.

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Diseases / indications

Drugs mentioned

  • SEREVENT DISKUS (SALMETEROL XINAFOATE)

Snippet

SUPPL AP for SEREVENT DISKUS (SALMETEROL XINAFOATE)