ENDARI® (L-Glutamine oral powder) July 8, 2017April 5, 2020 RR FDA Approvals Anemia - Sickle Cell The FDA on July 7, 2017 approved ENDARIĀ® for oral administration to reduce the acute complications of Sickle Cell disease, in adult and pediatric patients 5 years and older. ENDARIĀ® is a product of Emmaus Medical, Inc. Related Posts:FDA Approves ENDARI® for Sickle Cell DiseaseFDA Approves ENDARI®, A New Treatment for Sickle…FDA Approves Oral INQOVI® for Myelodysplastic SyndromesOral Apixaban for the Treatment of Acute Venous…Oral Relugolix Superior to Leuprolide in Advanced…Oral Bisphosphonates May Decrease the Risk of…