FDA
label_change
· 2022-01-06
FDA Approved: STRATTERA — Supplemental Application (Eli Lilly and Company)
Summary
The FDA approved a supplemental application for Strattera (atomoxetine hydrochloride) from Eli Lilly and Company, updating the drug's labeling.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for STRATTERA (ATOMOXETINE HYDROCHLORIDE)