FDA Approved Indications: Attention-Deficit/Hyperactivity Disorder (ADHD)
All FDA-approved indications unless otherwise excluded from Part D.
NA
NA
For initiation of treatment, a prior authorization form and relevant chart notes documenting medical rationale are required and for continuation of therapy, ongoing documentation of successful response to the medication may be necessary.
To obtain a prior authorization for atomoxetine, one or more of the following criteria must be met:
NA
Initial authorization and reauthorization will be approved for up to one year.