MYDAYIS
LOE Approachingdextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine aspartate monohydrate, and amphetamine sulfate
NDAORALCAPSULE, EXTENDED RELEASE
Approved
Jun 2017
Lifecycle
LOE Approaching
Competitive Pressure
15/100
Data completeness
3/8 — Basic
Drug data last refreshed 3h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MYDAYIS is an extended-release oral capsule combining four amphetamine salts (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine aspartate monohydrate, and amphetamine sulfate) approved in 2017. It is indicated for attention-deficit/hyperactivity disorder (ADHD) and works by stimulating central nervous system activity to improve focus, attention, and impulse control. The extended-release formulation provides once-daily dosing with a unique biphasic release profile designed for sustained symptom management throughout the day.
$0.003BPart D
LOE Approaching2.8 years to LOEWith LOE approaching in 2.9 years and modest Medicare spending ($3M in 2023), the brand team is likely consolidating and planning for generic transition; limited growth opportunity remains.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Why This Matters for Your Career
LOE in ~3 years — strategic planning for patent cliff underway
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.