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

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Summary

The FDA approved a supplemental application for SEREVENT DISKUS (salmeterol xinafoate) filed by GlaxoSmithKline LLC. This action updates the product’s labeling …

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Diseases / indications

• Asthma
• Chronic Obstructive Pulmonary Disease

Drugs mentioned

• SEREVENT DISKUS (SALMETEROL XINAFOATE)

Snippet

SUPPL AP for SEREVENT DISKUS (SALMETEROL XINAFOATE)