HYDERABAD, Dec 17 : Granules India Limited, a vertically integrated Indian pharmaceutical company, announced on Tuesday that its wholly-owned foreign subsidiary, Granules Pharmaceuticals, Inc. (GPI), has received approval from the U.S. Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Lisdexamfetamine Dimesylate Chewable Tablets for Attention Deficit Hyperactivity Disorder (AHD) treatment.
The approved drug is available in multiple strengths: 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, and 60 mg, Hyderabad based pharma company said in a release here.
This generic drug product has been determined to be bioequivalent (AB Rating) to the reference listed drug, Vyvanse? Chewable Tablets by Takeda Pharmaceuticals USA Inc.
Lisdexamfetamine dimesylate chewable tablets are indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients aged six years and older, as well as Moderate to Severe Binge Eating Disorder (BED) in adults.
Granules has received approval in the first review cycle, reflecting the company’s consistent focus on regulatory excellence and expedited product delivery.
Lisdexamfetamine Dimesylate Chewable Tablets are currently published on the FDA Drug Shortages List, emphasizing their critical role in patient care.
Commenting on the approval, Dr Krishna Prasad Chigurupati, Chairman & Managing Director of Granules Limited, said, ” With this approval, GPI reinforces its dedication to alleviating critical drug shortages in the U.S. healthcare market.”
Granules India Limited now holds 68 ANDA approvals, including 30 ANDAs from GPI.
(UNI)
The post Granules announces FDA approval for AHD treatment appeared first on Daily Excelsior.