At least 15 manufacturers have received approval for both capsule and chewable tablet generic versions of Vyvanse.
The FDA has approved the first generics of Takeda’s Vyvanse (lisdexamfetamine dimesylate) capsules and chewable tablets to treat attention-deficit/hyperactivity disorder (ADHD) in patients six years and older and moderate to severe binge-eating disorder in adults. Approvals have been given to 15 different manufacturers. The list of these new generics can be found here.
ADHD is one of the most common neurodevelopmental disorders of childhood, affecting about 10% of children, the FDA said in a press release. ADHD can be successfully managed with behavioral and pharmacological treatment, and some symptoms may improve as the child ages. Patients with binge-eating disorder have recurrent episodes of compulsive overeating. Binge eating disorder is the most common eating disorder in the United States, affecting about 1.25% of adult women and 0.42% of adult men, according to the National Institute of Diabetes and Digestive and Kidney Diseases.
Vyvanse was approved by the FDA in 2007 to treat patients with ADHD and in 2015 to treat patients with binge-eating disorder.
Vyvanse has experienced some shortages of some products, including the 60 mg capsules and 70 mg capsules in 100 count bottles, because of a manufacturing delay and increased demand, according to the American Society of Health-System Pharmacists. Takeda has Vyvanse 60 mg and 70 mg capsules on intermittent back order and the company estimates this will continue into September 2023.
In other generic news:
In this episode of the "Meet the Board" podcast series, Briana Contreras, Managed Healthcare Executive editor, speaks with Ateev Mehrotra, a member of the MHE editorial advisory board and a professor of healthcare policy and medicine at Harvard Medical School. Mehtrotra is also a hospitalist at the Beth Israel Deaconess Medical Center in Boston. In the discussion, Contreras gets to know Mehrotra more on a personal level and picks his brain on some of his research interests including telehealth, alternative payment models and price transparency.
Listen
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More