FDA
label_change
· 2009-01-15
FDA Approved: GLYBURIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
Summary
FDA approved a supplemental application for glyburide filed by Teva Pharmaceuticals USA, Inc., resulting in changes to the drug's labeling.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for GLYBURIDE (GLYBURIDE)