FDA
label_change
· 2007-02-10
FDA Approved: BYETTA — Supplemental Application (AstraZeneca Pharmaceuticals LP)
Summary
The FDA approved a supplemental application for BYETTA (exenatide) submitted by AstraZeneca, resulting in labeling changes for the drug.
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for BYETTA (EXENATIDE)