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FDA label_change · 2009-01-15

FDA Approved: GLYBURIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

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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

  • Glyburide (glyburide)

Snippet

SUPPL AP for GLYBURIDE (GLYBURIDE)