FDA
approval
· 2010-12-30
FDA Approved: SEREVENT DISKUS — Supplemental Application (GlaxoSmithKline LLC)
Summary
The FDA approved a supplemental application for SEREVENT DISKUS (salmeterol xinafoate) submitted by GlaxoSmithKline LLC.
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for SEREVENT DISKUS (SALMETEROL XINAFOATE)