drug
LISDEXAMFETAMINE DIMESYLATE
Marketedupdated 3mo agoby Actavis Elizabeth LLC
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 8- tagApproval112 co-mentions · 56 sources
- drugARYNTA97 co-mentions · 74 sources
- tagSmall Molecule56 co-mentions · 56 sources
- companySun Pharmaceutical Industries Ltd31 co-mentions · 10 sources
- tagRecall17 co-mentions · 10 sources
- companyOhm Laboratories Inc15 co-mentions · 8 sources
- tagDrug Shortage8 co-mentions · 8 sources
- companyApotex Corp1 co-mentions · 1 sources
all catalysts(5)
approval · 5
Aug 25, 2023
approval
LISDEXAMFETAMINE DIMESYLATE — FDA approval
LISDEXAMFETAMINE DIMESYLATE
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Jan 23, 2025
approval
LISDEXAMFETAMINE DIMESYLATE — FDA approval
LISDEXAMFETAMINE DIMESYLATE
→
Jun 16, 2025
approval
ARYNTA (LISDEXAMFETAMINE DIMESYLATE) — FDA approval
LISDEXAMFETAMINE DIMESYLATE
→
Dec 22, 2025
approval
ARYNTA (LISDEXAMFETAMINE DIMESYLATE) — FDA approval
LISDEXAMFETAMINE DIMESYLATE
→
Mar 18, 2026
approval
LISDEXAMFETAMINE DIMESYLATE — FDA approval
LISDEXAMFETAMINE DIMESYLATE
→
Trials studying LISDEXAMFETAMINE DIMESYLATE
- phase2Efficacy and Safety of Tirzepatide Versus Placebo or Lisdexamfetamine Dimesylate for Binge-Eating Disorder
- phase4Efficacy and Safety of Lisdexamfetamine Dimesylate in Adults With Chronic Fatigue Syndrome
- phase1To Compare and Evaluate the Oral Bioavailability of Lisdexamfetamine 70 mg Capsule With That of Elvanse® 70 mg Capsules, Hard Lisdexamfetamine Dimesylate in Healthy, Adult, Human Subjects Under Fasting Conditions.
- phase4Evaluation of the Effect and Safety of Lisdexamfetamine in Children Aged 6-12 With ADHD and Autism
Patent cliff
source: FDA Orange Bookfirst barrier falls
Apr 16, 2040
~13.7 years out
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (3)
- Aug 30, 2040formulationUS 11576878
- Apr 16, 2040formulationUS 12433859
- Apr 16, 2040formulationUS 12582620
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