FDA Approved: STRATTERA — Supplemental Application (Eli Lilly and Company)

View source ↗

Summary

FDA approves the supplemental application for Strattera (atomoxetine hydrochloride) submitted by Eli Lilly and Company.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

• Attention Deficit Hyperactivity Disorder

Drugs mentioned

• STRATTERA (Atomoxetine hydrochloride)

Snippet

SUPPL AP for STRATTERA (ATOMOXETINE HYDROCHLORIDE)