FDA Approved: ATOMOXETINE — Original Application (Teva Pharmaceuticals USA, Inc.)

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Summary

FDA approved Teva Pharmaceuticals USA, Inc.'s original ANDA for atomoxetine, establishing a generic version of the ADHD medication.

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Diseases / indications

• Attention Deficit Hyperactivity Disorder

Drugs mentioned

• Atomoxetine (Atomoxetine)

Snippet

ORIG AP for ATOMOXETINE (ATOMOXETINE)