QOL Medical, LLC Receives FDA Approval of Sucraid® (sacrosidase) Oral Solution Single-Use Containers for Patients with Congenital Sucrase-Isomaltase Deficiency (CSID)
Vero Beach, Florida—(PR NEWSWIRE)—QOL Medical, LLC, a ground-breaking, rare disease pharmaceutical company, announced today that the United States (U.S.) Food & Drug Administration (FDA) approved Sucraid® single-use containers for patients more than 33 lb (15 kg) with Congenital Sucrase-Isomaltase Deficiency
FDA Approves New Manufacturing Facility in Clearwater, Florida for Sacrosidase, Active Ingredient of Sucraid® (sacrosidase) Oral Solution, for the Treatment of Congenital Sucrase-Isomaltase Deficiency
October 2, 2018, Vero Beach, FL – Today QOL Medical, LLC announced that the U.S. Food and Drug Administration (FDA) has approved the company’s wholly owned manufacturing facility in Clearwater, Florida to manufacture sacrosidase, the drug substance used to make Sucraid® (sacrosidase) Oral Solution. The Sucraid® drug shortage has been resolved, and